CAS No.98-01-1,Furfural Suppliers,MSDS download

Hunan Russell Chemicals Technology Co.,Ltd

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China

furfural 98-01-1

Cas:98-01-1

Min.Order:0

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QINGDAO ON-BILLION INDUSTRAIL CO.,LTD

EINECSNO.202-626-1 FORMULAC5H6O2 MOLWT.98.10 H.S.CODE2932.13 TOXICITY Oral rat LD50: 177 mg/kg SYNONYMS 2-Furylmeth… Appearance:colorless to pale yellow liquid Storage:2-8°C Package:iso tank or 240kg drums Application:Furan polymers, in maki

Furfural

Cas:98-01-1

Min.Order:240 Kilogram

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Type:Trading Company

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Pure Chemistry Scientific Inc.

98-01-1 Application:Furfural

Furfural

Cas:98-01-1

Min.Order:0

Negotiable

Type:Trading Company

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Synthetic route

: 98-00-0
(2-furyl)methyl alcohol

: 98-01-1
furfural

Conditions

Conditions	Yield
With bis(2,2'-bipyridyl) copper(II) permanganate In acetone for 0.1h; Ambient temperature;	100%
With 4 A molecular sieve; tetrabutylammonium perchlorate; Ru-Cu-Al-hydrotalcite In toluene at 60℃; for 3h;	100%
With potassium carbonate In toluene at 70℃; for 2.5h; Reagent/catalyst;	100%

: 1899-24-7
5-bromo-2-furancarboxaldehyde

: 98-01-1
furfural

Conditions

Conditions	Yield
In diethyl ether for 1h; Product distribution; Irradiation; photochemical debromination was investigated;	100%

: Sodium; 6-{[1-furan-2-yl-meth-(E)-ylidene]-amino}-hexanoate

: 98-01-1
furfural

Conditions

Conditions	Yield
With hydrogenchloride for 0.0416667h; Product distribution; Ambient temperature; pH = 4-6, regeneration of aldehyde;	100%

: 613-75-2
(furan-2-yl)methylene diacetate

: 98-01-1
furfural

Conditions

Conditions	Yield
With sulphated zirconia In acetonitrile at 60℃; for 2h; Microwave irradiation;	100%
With Montmorillonite K10 In dichloromethane for 0.333333h; Heating;	98%
With water; Sulfate; titanium(IV) oxide In dichloromethane for 0.0833333h; Deacetylation; Heating;	97%

: 67421-75-4
2-(1,3-dithian-2-yl)furan

: 98-01-1
furfural

Conditions

Conditions	Yield
With dihydrogen peroxide; iodine; sodium dodecyl-sulfate In water at 20℃; for 1h; Micellar solution;	100%
With indium(III) trifluoride; water In acetonitrile for 3.5h; Reflux; chemoselective reaction;	93%
With 2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one; dihydrogen peroxide In water; acetonitrile at 20℃; for 0.75h;	90%
With eosin y In water; acetonitrile at 20℃; for 4h; Irradiation;	82%
With ammonium iodide; dihydrogen peroxide; sodium dodecyl-sulfate In water at 20℃; for 0.333333h; micellar medium;

: 18708-18-4
furfural tosylhydrazone

: 98-01-1
furfural

Conditions

Conditions	Yield
With Cr-MCM-41 zeolite on silica gel for 0.1h; microwave irradiation;	98%
With benzeneseleninic anhydride In tetrahydrofuran at 40 - 50℃; for 2h;	88%
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane; water at 20℃; for 2h; Oxidation; oxidative cleavage;	80%

: 58-86-6
D-xylose

: 98-01-1
furfural

Conditions

Conditions	Yield
With sulfonated graphitic carbon nitride In water at 100℃; for 0.5h; Solvent; Temperature;	96%
With Sulfonated graphene at 150℃; for 0.666667h; Temperature; Sealed tube;	96%
With hydrogenchloride; 5-methyl-dihydro-furan-2-one In water at 224.84℃; under 28443.9 Torr; for 0.0375h; Kinetics; Temperature; Reagent/catalyst; Concentration; Flow reactor;	93%

: 1708-41-4
2-(furan-2-yl)-1,3-dioxolane

: 98-01-1
furfural

Conditions

Conditions	Yield
With Montmorillonite K 10; water In acetone for 0.5h; Heating;	96%
With aluminum oxide; Oxone for 0.03h; Hydrolysis; Microwave irradiation;	93%
With iron(III) chloride hexahydrate; acetaldehyde In dichloromethane at 20℃; for 0.25h;	90%

: 1121-47-7
2-furaldehyde oxime

: 98-01-1
furfural

Conditions

Conditions	Yield
With water; Dess-Martin periodane In dichloromethane at 5℃; for 0.333333h;	95%
With silica gel; iron(III) chloride for 0.0133333h; microwave irradiation;	92%
With bis(pyridine)silver(I) permanganate In dichloromethane for 0.0833333h; Ambient temperature;	90%

: 117680-17-8
2-(Iodomethyl)tetrahydrofuran

: 98-01-1
furfural

Conditions

Conditions	Yield
With oxygen; kieselguhr; copper(l) chloride In hexane for 2h; Oxidation; Heating;	93%

: 2-(furan-2-ylmethylene)hydrazine-1-carboxamide

: 98-01-1
furfural

Conditions

Conditions	Yield
With aluminium trichloride; 1-benzyl-4-aza-1-azoniabicyclo[2.2.2]octane dichromate at 20℃; for 0.0125h;	93%
With sodium perborate In acetic acid at 40℃; for 1h; Oxidation;

: 6008-83-9
2-(1,3-dithiolan-2-yl)furan

: 98-01-1
furfural

Conditions

Conditions	Yield
Stage #1: 2-(1,3-dithiolan-2-yl)furan In ethanol at 20℃; Stage #2: With water In ethanol at 20℃;	93%
With indium(III) trifluoride; water In acetonitrile for 3.5h; Reflux; chemoselective reaction;	89%
With indium (III) iodide; dihydrogen peroxide In water; toluene at 20℃; for 15h; Inert atmosphere; Sealed tube;

: 81932-19-6
2-(furan-2-yl)-1,3-oxathiolane

: 98-01-1
furfural

Conditions

Conditions	Yield
Stage #1: 2-(furan-2-yl)-1,3-oxathiolane In ethanol at 20℃; Stage #2: With water In ethanol at 20℃;	93%
With copper(II) nitrate monohydrate at 90℃; for 0.333333h;	85%

: 2745-26-8
furan-2-yl-acetic acid

: 98-01-1
furfural

Conditions

Conditions	Yield
With potassium carbonate In chloroform at 20℃; for 24h; Irradiation; Inert atmosphere;	93%

: 14757-78-9
3-bromofurfural

: 98-01-1
furfural

Conditions

Conditions	Yield
In diethyl ether for 1h; Product distribution; Irradiation; photochemical debromination was investigated;	92%

: 10323-20-3
D-Arabinose

: 98-01-1
furfural

Conditions

Conditions	Yield
With Dowex 50Wx8-100 ion-exchange resin at 100℃; for 6h; Ionic liquid; Sealed tube;	92%
With silicoaluminophosphate-44 In water; toluene at 170℃; for 8h;	63%
With 1-butyl-3-methylimidazolium tetrachloridoferrate(III) In water; butanone at 160℃; for 3h;	50.7%

: 534-22-5
2-methylfuran

: 98-01-1
furfural

Conditions

Conditions	Yield
With nickel-doped graphene carbon nitride nanoparticles; air In ethanol at 25℃; for 8h; Irradiation; Green chemistry;	92%
With oxygen In acetonitrile at 20℃; for 18h; Irradiation;	95 %Spectr.
With tert.-butylhydroperoxide; C29H25Cl2N4Ru(1+)*F6P(1-) In acetonitrile at 60℃; for 3h; Schlenk technique; Inert atmosphere;	71 %Chromat.

: 1949-78-6
L-lyxose

: 98-01-1
furfural

Conditions

Conditions	Yield
With 1-methyl-3-(4-sulfobutyl)-1H-imidazol-3-ium hydrogensulfate; 4-methyl-2-pentanone In water at 150℃; under 760.051 Torr; for 0.416667h; Autoclave;	91.4%

: 108-29-2
5-methyl-dihydro-furan-2-one

: 98-01-1
furfural

Conditions

Conditions	Yield
With D-Xylose In water at 180℃; for 0.666667h; Temperature; Reagent/catalyst;	91.4%

: 2460-44-8
β-D-xylopyranoside

: 98-01-1
furfural

Conditions

Conditions	Yield
With phosphorus and fluorine co-doped amorphous carbon nitride In tetrahydrofuran; water at 130℃; for 5h;	91%
With hydrogen In water at 150℃; under 750.075 Torr; Temperature;	87.6%
With vanadyl pyrophosphate In water; toluene at 170℃; for 6h;	56%

: 539-47-9
3-(2-furyl)acrylic acid

: 98-01-1
furfural

Conditions

Conditions	Yield
With aluminum oxide; potassium permanganate In dichloromethane at 20℃;	90%

: 1027382-27-9
tert-butyldimethyl(2,2,2-trichloro-1-furan-2-ylethoxy)silane

: 98-01-1
furfural

Conditions

Conditions	Yield
With tetrabutyl ammonium fluoride In tetrahydrofuran; N,N-dimethyl-formamide at 50℃;	90%

: 6270-56-0
2-(ethoxymethyl)furan

: 98-01-1
furfural

Conditions

Conditions	Yield
With water; 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate In acetonitrile at 20℃; for 8h;	90%

: 71778-41-1
2-(bis(phenylthio)methyl)furan

: 98-01-1
furfural

Conditions

Conditions	Yield
With indium(III) trifluoride; water In acetonitrile for 3h; Reflux; chemoselective reaction;	90%

: 50-69-1
D-ribose

: 98-01-1
furfural

Conditions

Conditions	Yield
With Dowex 50Wx8-200 ion-exchange resin at 100℃; for 3h; Ionic liquid; Sealed tube;	90%
With 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate; copper dichloride at 120℃; for 0.3h; Reagent/catalyst; Ionic liquid;	67 %Chromat.

: 709-10-4
2-(furan-2-yl)-5,5-dimethyl-1,3-dioxane

: 98-01-1
furfural

Conditions

Conditions	Yield
With indium(III) trifluoride; water In acetonitrile for 2.5h; Reflux; chemoselective reaction;	89%

: 527-69-5
2-furancarbonyl chloride

: 98-01-1
furfural

Conditions

Conditions	Yield
With pentacoordinated hydrogenosilane 1	87%
With bis(triphenylphosphine)copper(I) tetrahydroborate; triphenylphosphine In acetone at 25℃; for 1h;	78%
With tert-butyl isocyanide; CpRu(PiPr3)(CH3CN)2PF6; Dimethylphenylsilane In [(2)H6]acetone at 20℃; for 24h; chemoselective reaction;	100 %Spectr.
With tert-butyl isocyanide; CpRu(PiPr3)(CH3CN)2PF6; Dimethylphenylsilane In [(2)H6]acetone at 20℃; for 24h; chemoselective reaction;	Ca. 100 %Spectr.

: 1453-62-9
2-furaldehyde dimethyl acetal

: 98-01-1
furfural

Conditions

Conditions	Yield
With indium(III) trifluoride; water In acetonitrile for 2h; Reflux; chemoselective reaction;	87%
indium(III) chloride In methanol; water for 2h; Heating;	85%

: 617-89-0
furan-2-ylmethanamine

: 98-01-1
furfural

Conditions

Conditions	Yield
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene In dichloromethane at 0 - 20℃; for 0.333333h; Inert atmosphere; Green chemistry;	87%
With pyridoxal 5'-phosphate; sodium pyruvate In aq. phosphate buffer at 30℃; pH=7.5; Reagent/catalyst; Enzymatic reaction;

: 620-03-1
furan-2-carbaldehyde oxime

: 98-01-1
furfural

Conditions

Conditions	Yield
With manganese triacetate In benzene for 1h; Heating;	86%
With antimonypentachloride In dichloromethane at 20℃; for 2.3h;	75%

: 98-01-1
furfural

: 108-94-1
cyclohexanone

: 62085-75-0
(2E,6E)-2,6-bis(2-furylmethylene)cyclohexanone

Conditions

Conditions	Yield
With sodium hydroxide In ethanol for 0.025h; microwave irradiation;	100%
With sodium hydroxide In ethanol; water at 20℃; for 24h; Inert atmosphere; Green chemistry;	99%
aluminum oxide for 0.0416667h; microwave irradiation;	98%

: 98-01-1
furfural

: 106-49-0
p-toluidine

: 13060-72-5
furfurylidene-p-toluidine

Conditions

Conditions	Yield
In methanol at 20℃; for 24h;	100%
In methanol at 20℃; for 24h;	100%
In methanol at 20℃;	85%

: 98-01-1
furfural

: 104-94-9
4-methoxy-aniline

: 1749-14-0, 100239-11-0
N-furfurylidene-p-anisidine

Conditions

Conditions	Yield
With sodium sulfate In benzene for 0.5h; Ambient temperature;	100%
In methanol at 20℃; for 24h;	100%
In methanol at 20℃; for 24h;	100%

: 98-01-1
furfural

: 62-53-3
aniline

: 3237-23-8
N-(2-furylmethylene)aniline

Conditions

Conditions	Yield
With copper(II) bis(trifluoromethanesulfonate) In water at 20℃; for 0.0166667h;	100%
With aluminum oxide for 5h; Milling;	100%
sodium hydrogen sulfate; silica gel at 56 - 58℃; for 0.0244444h; microwave irradiation;	98%

: 98-01-1
furfural

: 762-04-9
phosphonic acid diethyl ester

: 20627-09-2
diethyl (hydroxy(furan-2-yl)methyl)phosphonate

Conditions

Conditions	Yield
With triethylamine In neat (no solvent) at 20℃; Pudovik Reaction; Inert atmosphere;	100%
With triethylamine at 50℃; Pudovik Reaction; Inert atmosphere; Sealed tube;	100%
With 2-tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine supported on polystyrene In neat (no solvent) at 30℃; for 3h; Pudovik Reaction; Green chemistry;	99%

: 98-01-1
furfural

: 105-56-6
ethyl 2-cyanoacetate

: 67449-75-6, 23973-22-0
ethyl (E)-2-cyano-3-(2-furyl)-2-propenoate

Conditions

Conditions	Yield
With L-proline for 0.0333333h; Knoevenagel condensation; microwave irradiation;	100%
ytterbium(III) perfluorooctanesulfonate In toluene at 80℃; for 3h; Knoevenagel condensation;	99%
With polyacrylonitrile fiber modified with triethylenetetramine In water at 50℃; for 1.5h; Knoevenagel condensation;	99%

: 98-01-1
furfural

: 91-59-8
naphthalen-2-ylamine

: 6233-18-7
(E)-1-(furan-2-yl)-N-(naphthalen-2-yl)methanimine

Conditions

Conditions	Yield
In diethyl ether at 20℃; Inert atmosphere; Molecular sieve; Darkness;	100%

: 98-01-1
furfural

: 123-54-6
acetylacetone

: 4728-04-5
3-(furan-2-ylmethylene)pentane-2,4-dione

Conditions

Conditions	Yield
With piperidine; acetic acid In dichloromethane at 0 - 20℃; Michael Addition; Molecular sieve;	100%
With L-Lysine hydrochloride; triethylamine In N,N-dimethyl-formamide at 20℃; for 3h; Knoevenagel Condensation;	98.3%
With cross-linked polystyrene-titanium tetrachloride complex In neat (no solvent) at 60℃; for 2h; Knoevenagel Condensation;	98%

: 98-01-1
furfural

: 100-46-9
benzylamine

: 4393-11-7
N-benzyl-1-(furan-2-yl)methanimine

Conditions

Conditions	Yield
With copper(II) bis(trifluoromethanesulfonate) In water at 20℃; for 0.0166667h;	100%
In water at 20℃; for 2h;	93%
In dichloromethane Inert atmosphere; Molecular sieve;	81%

: 98-01-1
furfural

: 109-77-3
malononitrile

: 3237-22-7
2-cyano-3-(2-furanyl)acrylonitrile

Conditions

Conditions	Yield
With 1-butyl-1,4-diazabicyclo[2.2.2]octanylium hydrotetrafluoroborate In water at 20℃; for 0.0166667h; Knoevenagel condensation;	100%
With 1,4-diaza-bicyclo[2.2.2]octane In water at 20℃; for 0.0166667h; Knoevenagel Condensation; Green chemistry;	100%
With hydroquinone; p-benzoquinone In water at 20℃; for 3h; Reagent/catalyst; Knoevenagel Condensation; Inert atmosphere; Sealed tube;	100%

: 98-01-1
furfural

: 149-73-5
trimethyl orthoformate

: 1453-62-9
2-furaldehyde dimethyl acetal

Conditions

Conditions	Yield
With Yb(III)-coordinated adamantane-based porous polymer In methanol at 20℃; for 12h; Catalytic behavior; Reagent/catalyst;	100%
indium(III) triflate In dichloromethane at 20℃; for 0.0833333h;	99%
With cerium triflate In methanol at 20℃; for 0.0333333h;	99%

: 98-01-1
furfural

: 97-99-4
Tetrahydrofurfuryl alcohol

Conditions

Conditions	Yield
With hydrogen In ethanol at 60℃; under 15001.5 Torr; for 4h; Catalytic behavior; Reagent/catalyst; Temperature; Solvent; Pressure; Autoclave; Green chemistry;	100%
With hydrogen In butan-1-ol at 80℃; under 30003 Torr; for 5h; Catalytic behavior; Temperature; Reagent/catalyst;	99%
With hydrogen In isopropyl alcohol at 179.84℃; under 22502.3 Torr; for 1.25h; Reagent/catalyst;	99%

: 98-01-1
furfural

: 534-22-5
2-methylfuran

Conditions

Conditions	Yield
With hydrogen under 2250.23 Torr; for 15h;	100%
With hydrogen at 200℃; under 760.051 Torr;	95.5%
With hydrogen at 120℃; under 760.051 Torr; for 24h; Catalytic behavior; Reagent/catalyst; Temperature;	94.5%

: 98-01-1
furfural

: 98-00-0
(2-furyl)methyl alcohol

Conditions

Conditions	Yield
With Pt(3)Co(3)/C; hydrogen In water at 35℃; under 750.075 Torr; for 10h; Reagent/catalyst; Pressure; Temperature; Solvent; Concentration;	100%
With HRO/TiO2; hydrogen In water at 150℃; under 15001.5 Torr; for 3h;	100%
With hydrogen In isopropyl alcohol at 179.84℃; under 22502.3 Torr; for 1.25h; Reagent/catalyst;	100%

: 98-01-1
furfural

: 14032-66-7
5-hydroxy-2-(5H)-furanone

Conditions

Conditions	Yield
With methanol; oxygen Irradiation;	100%
With oxygen; methylene blue In methanol at -78 - 20℃; for 23h; Irradiation;	98%
With oxygen; Rose Bengal lactone In methanol at 20℃; for 24h; Photolysis;	93%

: 98-01-1
furfural

: 617-89-0
furan-2-ylmethanamine

Conditions

Conditions	Yield
With ammonia; hydrogen In tetrahydrofuran at 80℃; for 2h; Autoclave;	100%
With ammonia; hydrogen In methanol at 30℃; for 24h; Autoclave;	91%
With ammonium hydroxide; Ni6AlO(z); hydrogen at 100℃; under 3000.3 Torr; for 5h; Autoclave;	90%

: 98-01-1
furfural

: 620-03-1
furan-2-carbaldehyde oxime

Conditions

Conditions	Yield
With pyridine; hydroxylamine hydrochloride In ethanol	100%
With hydroxylamine hydrochloride In ethanol; water for 0.166667h; Microwave irradiation;	89%
With N-hydroxyphthalimide In water at 90℃; for 3h; Sealed tube;	89%

: 98-01-1
furfural

: 4464-77-1, 69314-24-5, 69314-25-6, 116204-42-3
1,2-di-furan-2-yl-ethane-1,2-diol

Conditions

Conditions	Yield
With tris(2,2’-bipyridine)ruthenium(II); ascorbate In water for 3h; pH=12.7; Irradiation;	100%
With ammonium chloride; magnesium Ambient temperature;	92%
With triethylammonium formate; magnesium In methanol; water at 25℃; for 0.333333h;	74%

: 98-01-1
furfural

: 109-80-8
1.3-propanedithiol

: 67421-75-4
2-(1,3-dithian-2-yl)furan

Conditions

Conditions	Yield
With lithium tetrafluoroborate at 0℃; for 5h;	100%
With amberlyst-15 In acetonitrile for 1h;	99.92%
With dimethylbromosulphonium bromide at 20℃; for 0.0833333h;	98%

: 98-01-1
furfural

: 867-13-0
diethoxyphosphoryl-acetic acid ethyl ester

: 623-20-1
ethyl (E)-3-(2-furyl)prop-2-enoate

Conditions

Conditions	Yield
With potassium carbonate In neat (no solvent) Mechanism; var. other bases, effect of water;	100%
With water; barium dihydroxide In 1,4-dioxane at 70℃; for 0.416667h;	100%
With water; barium dihydroxide In 1,4-dioxane at 70℃; for 0.416667h; Product distribution; other catalyst, other solvents, influence of water;	100%

: 98-01-1
furfural

: 74-90-8
hydrogen cyanide

: 10017-07-9
(S)-2-(2'-furyl)-2-hydroxy-acetonitrile

Conditions

Conditions	Yield
With (R)-oxynitrilase (almond meal) In di-isopropyl ether at 4℃; for 48h;	100%
With almond meal ((R)-oxynitrilase) In di-isopropyl ether at 4 - 30℃;	100%
With almond meal In di-isopropyl ether at 15℃;	100%

: 98-01-1
furfural

: 7677-24-9
trimethylsilyl cyanide

: 40861-56-1
2-(2-furyl)-2-(trimethylsilyloxy)acetonitrile

Conditions

Conditions	Yield
With Eu2(benzene-1,2,3,4,5,6-hexacarboxylate)(H2O)3 In acetonitrile at 20 - 100℃; for 1h;	100%
With 1-methoxy-2-methyl-1-(trimethylsiloxy)propene at 19℃; for 10h;	99%
With potassium phtalimide at 20℃; for 1.16667h; solvent-free;	99%

: 98-01-1
furfural

: 2537-48-6
diethyl 1-cyanomethylphosphonate

: 6125-63-9
(E)-3-(2-furyl)acrylonitrile

Conditions

Conditions	Yield
With water; barium dihydroxide In 1,4-dioxane at 70℃; for 0.666667h;	100%
Stage #1: diethyl 1-cyanomethylphosphonate With sodium hydride In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Stage #2: furfural In tetrahydrofuran at 28℃;
Stage #1: diethyl 1-cyanomethylphosphonate With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.5h; Stage #2: furfural In tetrahydrofuran; mineral oil at 0 - 25℃; for 2h;

: 98-01-1
furfural

: 45732-93-2
1-(Hydroxyaminomethyl)-1-cyclohexanol

: 84966-16-5
N-Furfuryliden-(1-hydroxycyclohexyl)methanamin-N-oxid

Conditions

Conditions	Yield
In ethanol Ambient temperature;	100%

: 98-01-1
furfural

: 56613-80-0
(R)-Phenylglycinol

: 139437-47-1
(R)-2-{[1-Furan-2-yl-meth-(E)-ylidene]-amino}-2-phenyl-ethanol

Conditions

Conditions	Yield
With magnesium sulfate In dichloromethane at 20℃; for 12h;	100%
In benzene Heating;	88%
In benzene Heating;	85%
With magnesium sulfate In dichloromethane
In toluene Condensation; Heating;

: 98-01-1
furfural

: 3084-53-5
trimethylsulphonium bromide

: 2745-17-7
2-furyloxirane

Conditions

Conditions	Yield
With potassium hydroxide In neat (no solvent) Mechanism; var. other bases, effect of water;	100%
With potassium hydroxide In water; acetonitrile	98%
With potassium hydroxide; water In acetonitrile at 40℃; for 0.833333h; Product distribution;	93%

: 98-01-1
furfural

: 1826-67-1
vinyl magnesium bromide

: 119619-38-4
1-(furan-2-yl)-2-propen-1-ol

Conditions

Conditions	Yield
In tetrahydrofuran at 0℃; for 1h; Inert atmosphere;	100%
In tetrahydrofuran at 0 - 20℃; Inert atmosphere;	98%
In tetrahydrofuran at 0 - 20℃; Inert atmosphere;	92%

: 98-01-1
furfural

: 143-33-9
sodium cyanide

: 541-41-3
chloroformic acid ethyl ester

: 20893-23-6
carbonic acid, cyano(2-furyl)methyl ethyl ester

Conditions

Conditions	Yield
With tetrabutyl-ammonium chloride In dichloromethane; water Heating;	100%

...Expand

: 98-01-1
furfural

: 536-90-3
m-Anisidine

: 95124-20-2
N-(furan-2-ylmethylene)-3-methoxyaniline

Conditions

Conditions	Yield
In methanol at 20℃; for 24h;	100%
for 2h; Yield given;
With magnesium sulfate In ethanol at 20℃;

: 98-01-1
furfural

: 34164-50-6
4-penten-1-ylmagnesium bromide

: 106549-86-4, 84735-65-9
(+/-)-1-(furan-2-yl)hex-5-en-1-ol

Conditions

Conditions	Yield
In tetrahydrofuran at 0℃;	100%
In tetrahydrofuran at 0 - 20℃; for 2h; Inert atmosphere;	86%
In tetrahydrofuran at 0℃;	73%

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