CAS No.106-95-6,Allyl bromide Suppliers,MSDS download

Jinan Finer Chemical Co., Ltd

Product description: Product name Allyl bromide CAS number 106-95-6 Assay ≥99% Appearance Colorless transparent liquid Capacity 1000mt/year Application Dye, spice, pesticide

Allyl bromide

Cas:106-95-6

Min.Order:1 Kilogram

FOB Price: $12.0

Type:Lab/Research institutions

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Lonwin Chemical Group Limited

Allyl bromide CAS: 106-95-6 Specification Product name Allyl bromide CAS number 106-95-6 Assay ≥99% Appearance Colorless transparent liquid Capacity 1000mt/year Applicat

Factory supply Allyl bromide

Cas:106-95-6

Min.Order:1 Kilogram

Negotiable

Type:Other

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Hunan Russell Chemicals Technology Co.,Ltd

low price and high purityAppearance:solid or liquid Storage:in sealed air resistant place Package:As customer require Application:Pharma;Industry;Agricultural Transportation:by sea or by airplane Port:any port in China

Allyl bromide, 99%, stabilized 106-95-6

Cas:106-95-6

Min.Order:0

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Type:Trading Company

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Amadis Chemical Co., Ltd.

1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G

Amadis Chemical offer CAS#106-95-6;CAT#A801548

Cas:106-95-6

Min.Order:10 Milligram

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QINGDAO ON-BILLION INDUSTRAIL CO.,LTD

ProductName:Allylbromide Synonyms:1-Bromo-2-propene;1-Propene,3-bromo-;3-bromo-1-propen;3-bromo-prop-1-ene;3-bromo-propen;3-Brompropen;Allylbro… Appearance:clear liquid Storage:store at RT Package:250kg drums Application:organic synthesis i

Allyl bromide

Cas:106-95-6

Min.Order:250 Kilogram

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Type:Trading Company

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Synthetic route

: Ru(η5-C5H5)-(η3-C3H5)Br2

A: bromodicarbonyl(η5-cyclopentadienyl)ruthenium

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With CO In decane (CO); heating (6 h, 140°C), cooling; chromy. (silica gel, ether);	A 97% B n/a
With CO In decane (CO); heating (2 h, 140°C), cooling; chromy. (silica gel, ether);	A 48% B n/a

: (η5-C5Me5)RuBr2(η3-allyl)

A: 90420-05-6
{(η5-C5(CH3)5)Ru(CO)2Br}

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With CO In decane (CO); heating (2 h, 140°C), cooling; chromy. (silica gel, ether);	A 96% B n/a
With CO In decane (CO); heating (2 h, 120°C), cooling; chromy. (silica gel, ether);	A 45% B n/a
With carbon monoxide In diethylene glycol heating in diglime under CO atm.;;	A 70-80 B 50-70

: Ru(η5-C5H5)-(η3-C3H5)Br2

: 106-42-3
para-xylene

A: (η5-C5H5)Ru(p-xylene)Br

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
(N2); heating (16 h, 140°C), cooling; concn., chromy. (silica gel, MeOH); elem. anal.;	A 94% B n/a

...Expand

: 107-11-9
1-amino-2-propene

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With para-bromotoluene; oxalic acid at 65℃; for 1.33333h; Temperature; Reflux;	93%

: 106-96-7
propargyl bromide

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With piperazine; hydrogen In ethanol at 80℃; under 4500.45 Torr; for 24h;	92%
With piperazine; hydrogen In ethanol at 100℃; under 4500.45 Torr; for 24h; Green chemistry;
With hydrogen In ethanol at 100℃; under 4500.45 Torr; for 24h; chemoselective reaction;	89 %Chromat.
With hydrogen In ethanol at 30℃; under 3750.38 Torr; for 2h; chemoselective reaction;

: 107-18-6
allyl alcohol

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With silica bromide In dichloromethane at 20℃; for 0.0833333h;	91%
With Silphos; bromine In acetonitrile for 0.166667h; Heating;	84%
With tetradecafluorohexane; phosphorus tribromide In diethyl ether at 20℃; for 12h;	75%

: 96-11-7
1,2,3-tribromopropane

A: 106-95-6
allyl bromide

B: bromo(hexaethyltriamino)phosphonium bromide

Conditions

Conditions	Yield
With hexaethylphosphoric triamide In benzene for 24h; Ambient temperature; Yields of byproduct given;	A 89.9% B n/a

: 369594-22-9
6,7-dihydropyrido[3,2,1-ij]quinazoline-1,3 (2H,5H)-dione

A: 1422210-23-8
2-allyl-6,7-dihydro-5H-pyrido[3,2,1-ij]quinazoline-1,3-dione

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
	A n/a B 89%

: 76065-47-9
C17H19BrO2Te

A: 24727-22-8
dibromo-bis-(4-methoxy-phenyl)-λ4-tellane

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With bromine at 0℃; for 4h;	A 80% B n/a

: 107-05-1
3-chloroprop-1-ene

A: 78-75-1
1,2-Dibromopropane

B: 3017-96-7
1-bromo-2-chloropropane

C: 3017-95-6, 127054-44-8, 130232-86-9
2-bromo-1-chloropropane

D: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With hydrogen bromide; ferric(III) bromide In dichloromethane at 25℃; for 0.5h;	A 79% B 16% C 2% D 2%

...Expand

: 498-62-4
3-thiophene carboxaldehyde

: 100-39-0
benzyl bromide

: 123-11-5
4-methoxy-benzaldehyde

A: 106-95-6
allyl bromide

B: 220338-01-2
3-((Z)-2-Benzylsulfanyl-vinyl)-5-(4-methoxy-phenyl)-2,5-dihydro-furan-2-ol

Conditions

Conditions	Yield
With samarium; 1,2-Diiodoethane In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide for 27h; Ambient temperature;	A 22% B 63%

...Expand

: 506-68-3
bromocyane

: 76065-43-5
allyldiphenyltelluronium bromide

A: 76065-55-9
C13H10BrNTe

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
at 25℃; for 8h;	A 62% B n/a

...Expand

: 18146-00-4
allyloxytrimethylsilane

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With Tri-n-butylfluorphosphoniumbromid In dichloromethane at 20℃; for 24h;	61%

: 105900-07-0
trans-{Me2Co(11-hydroxy-2,3,9,10-tetramethyl-1,4,8,11-tetraazaundeca-1,3,8,10-tetraen-1-olate)}

: 100-39-0
benzyl bromide

A: 103-29-7
1,1'-(1,2-ethanediyl)bisbenzene

B: 106-95-6
allyl bromide

C: 108-88-3
toluene

Conditions

Conditions	Yield
In [D3]acetonitrile Kinetics; Irradiation (UV/VIS); Degasses condition, 298 K, 33 h;; detected by NMR-spectroscopy;;	A 22% B n/a C 55%

...Expand

: 25360-57-0
{EtCobis(dimethylglyoximato)(pyridine)}

: 100-39-0
benzyl bromide

A: 106-95-6
allyl bromide

B: 108-88-3
toluene

Conditions

Conditions	Yield
In [D3]acetonitrile Kinetics; Irradiation (UV/VIS); Degasses condition, 298 K, 14 h;; detected by NMR-spectroscopy;;	A n/a B 33%

...Expand

: 109-64-8
1,3-dibromo-propane

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With sodium hydroxide; cetylpyridinium bromide at 130℃; for 2h;	20%
With silver(l) oxide
With Hexamethylphosphorous triamide

: 23642-14-0
{MeCobis(dimethylglyoximato)(pyridine)}

: 100-39-0
benzyl bromide

A: 106-95-6
allyl bromide

B: 108-88-3
toluene

Conditions

Conditions	Yield
In [D3]acetonitrile Kinetics; Irradiation (UV/VIS); Degasses condition, 298 K, 71 h;; detected by NMR-spectroscopy;;	A n/a B 6.4%

...Expand

: N-allyl-N-[2]thienylmethyl-aniline

: 506-68-3
bromocyane

: 106-95-6
allyl bromide

: 187737-37-7
propene

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With bromine at 300 - 315℃;
With N-Bromosuccinimide; toluene-4-sulfonic acid In tetrahydrofuran at 100℃; for 4h; Inert atmosphere; Schlenk technique;
With bromine at 525℃;

: 506-68-3
bromocyane

: 31930-96-8
N-allyl-N-benzylaniline

A: 25855-25-8
N-benzyl-N-phenylcyanamide

B: 106-95-6
allyl bromide

...Expand

: 1838-59-1
3-formyloxy-propene

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With hydrogen bromide; zinc Darst.;

: 100-39-0
benzyl bromide

: 107-18-6
allyl alcohol

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With triphenyl phosphite at 140℃;

: 39943-76-5
dibromotriphenoxyphosphorane

: 107-18-6
allyl alcohol

: 106-95-6
allyl bromide

: 110-52-1
1,4-dibromo-butane

: 34557-54-5
methane

: 14604-48-9
vinyl cation

A: 187737-37-7
propene

B: 463-49-0
1,2-propanediene

C: 106-94-5
propyl bromide

D: 106-95-6
allyl bromide

Conditions

Conditions	Yield
at 100℃; under 60 - 720 Torr; Product distribution; Kinetics; Thermodynamic data; labelled with tritium; -ΔH;

...Expand

: 110-52-1
1,4-dibromo-butane

: 463-49-0
1,2-propanediene

A: 557-93-7
2-bromoprop-1-ene

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With water; hydrogen; oxygen at 37℃; under 150 Torr; Product distribution; Irradiation; variation of system composition and initial pressure;

...Expand

: 110-52-1
1,4-dibromo-butane

: 1724-46-5, 1981-80-2, 6067-68-1, 15552-77-9, 50457-57-3, 50457-58-4, 65887-19-6, 65887-20-9
prop-1->3-enylium

A: 22211-90-1
bromolanium

B: 106-95-6
allyl bromide

Conditions

Conditions	Yield
Mechanism; Irradiation;

...Expand

: 1981-80-2, 13932-24-6
allyl radical

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With bromine under 1 Torr; Rate constant; concentration dependence; reaction of allyl radicals with NO2;
With bromine at 24.9 - 258.9℃; Kinetics; Irradiation; carrier gas, He, the role of resonance stabilization;

: 556-56-9
allyl iodid

: 106-95-6
allyl bromide

Conditions

Conditions	Yield
With pyridine; tributyltin bromide at 50℃; Thermodynamic data; Equilibrium constant; Δ G;	20 % Chromat.
With bismuth(III) bromide In 1,2-dichloro-ethane for 1.75h; Heating; Yield given;

: 148-24-3
8-quinolinol

: 106-95-6
allyl bromide

: 7652-26-8
8-Allyloxy-chinolin

Conditions

Conditions	Yield
With potassium carbonate In acetone for 24h; Heating;	100%
With sodium hydroxide; tetrabutylammomium bromide In dichloromethane; water at 25℃; for 4h;	84%
With potassium carbonate In ethanol at 70℃; for 10h; regioselective reaction;	84%

: 93-35-6
7-hydroxy-2H-chromen-2-one

: 106-95-6
allyl bromide

: 31005-03-5
7-allyloxycoumarin

Conditions

Conditions	Yield
With potassium carbonate In acetone for 5h; Heating;	100%
Stage #1: 7-hydroxy-2H-chromen-2-one With potassium carbonate In acetone at 20℃; for 0.0833333h; Stage #2: allyl bromide In acetone for 3h; Reflux;	100%
With potassium carbonate In acetone at 70℃; for 12h;	98.6%

: 90-33-5, 79566-13-5
7-hydroxy-4-methyl-chromen-2-one

: 106-95-6
allyl bromide

: 3993-57-5
7-allyloxy-4-methyl-2H-chromen-2-one

Conditions

Conditions	Yield
With potassium carbonate In acetone at 60℃; for 1h; regioselective reaction;	100%
With potassium carbonate In acetone for 16h; Reflux;	90%
With potassium carbonate In acetone for 12h; Reflux;	90%

: 92-84-2
10H-phenothiazine

: 106-95-6
allyl bromide

: 20962-92-9
10-allylphenothiazine

Conditions

Conditions	Yield
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In various solvent(s) for 2.5h; Ambient temperature;	100%
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane for 3h; Product distribution; Ambient temperature; other solvent;	90%
	87%
With sodium hydroxide; tetrabutylammomium bromide In toluene	62%
With copper; sodium carbonate; benzene

: 108-94-1
cyclohexanone

: 106-95-6
allyl bromide

: 1123-34-8
1-allyl-1-cyclohexanol

Conditions

Conditions	Yield
With ammonium acetate; zinc In tetrahydrofuran at 0℃; for 0.166667h; Inert atmosphere;	100%
zinc In N,N-dimethyl-formamide for 2h; Product distribution; Ambient temperature; other solvents : N,N-dimethylacetoamide, N-methyl-2-pyrrolidone, 2-pyrrolidone, 2-methyloxazoline;	99%
With zinc In N,N-dimethyl-formamide for 2h; Ambient temperature; other solvents : N,N-dimethylacetoamide, N-methyl-2-pyrrolidone, 2-pyrrolidone, 2-methyloxazoline;	99%

: 767-00-0
4-cyanophenol

: 106-95-6
allyl bromide

: 33148-47-9
4-allyloxy-benzonitrile

Conditions

Conditions	Yield
With caesium carbonate In water; N,N-dimethyl-formamide at 20℃; for 12h;	100%
With potassium carbonate In acetone at 20℃; for 24h;	99%
With potassium carbonate In acetone at 20℃; for 20h; Reflux;	98%

: 100-52-7
benzaldehyde

: 106-95-6
allyl bromide

: 80735-94-0
1-Phenyl-3-buten-1-ol

Conditions

Conditions	Yield
With zinc In tetrahydrofuran at 20℃; for 1h; Alkylation; Barbier allylation;	100%
With potassium fluoride; antimony In water for 16h; allylation;	100%
With hydrogenchloride; antimony In water for 16h; Product distribution; Further Variations:; Reagents; times;	100%

: 123-08-0
4-hydroxy-benzaldehyde

: 106-95-6
allyl bromide

: 40663-68-1
4-(2-propenyloxy)benzaldehyde

Conditions

Conditions	Yield
With potassium carbonate In acetone at 65℃;	100%
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide at 20℃; for 6h;	100%
With tetra-(n-butyl)ammonium iodide; potassium carbonate In N,N-dimethyl-formamide at 20℃; for 6h;	100%

: 90-02-8
salicylaldehyde

: 106-95-6
allyl bromide

: 28752-82-1
2-(allyloxy)benzaldehyde

Conditions

Conditions	Yield
With potassium carbonate In acetone for 9h; Reflux;	100%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;	100%
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 1h;	100%

: 148-53-8
3-methoxy-2-hydroxybenzaldehyde

: 106-95-6
allyl bromide

: 23343-06-8
2-allyloxy-3-methoxy-benzaldehyde

Conditions

Conditions	Yield
With potassium carbonate In acetone at 50℃; Williamson Ether Synthesis;	100%
With sodium hydroxide; benzyltri(n-butyl)ammonium chloride In dichloromethane Ambient temperature;	98%
With potassium carbonate In acetonitrile for 4h; Inert atmosphere; Reflux;	98%

: 108-98-5
thiophenol

: 106-95-6
allyl bromide

: 5296-64-0
allyl phenyl thioether

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 20℃;	100%
With silica gel In water at 20℃; for 1h;	95%
With potassium fluoride on Celite In acetonitrile at 83℃; for 2h;	95%

: 100-83-4
meta-hydroxybenzaldehyde

: 106-95-6
allyl bromide

: 40359-32-8
3-allyloxy-benzaldehyde

Conditions

Conditions	Yield
With potassium carbonate In acetone for 18h; Heating;	100%
With potassium carbonate; sodium iodide In ethanol for 3h; Reflux;	100%
With potassium carbonate In ethanol for 3h; Reflux;	100%

: 150-76-5
4-methoxy-phenol

: 106-95-6
allyl bromide

: 13391-35-0
allyl (4-methoxyphenyl) ether

Conditions

Conditions	Yield
With potassium carbonate In butanone for 12h; Heating;	100%
With potassium carbonate In acetone at 20℃; Reflux;	100%
With potassium carbonate In acetone Reflux;	99%

: 90-05-1
2-methoxy-phenol

: 106-95-6
allyl bromide

: 4125-43-3
O-allyl guaiacol

Conditions

Conditions	Yield
With potassium carbonate In acetone at 20℃; Reflux;	100%
With potassium carbonate; potassium iodide In acetone for 18h; Reflux;	100%
With potassium carbonate	99%

: 99-76-3
methyl 4-hydroxylbenzoate

: 106-95-6
allyl bromide

: 35750-24-4
methyl 4-allyloxybenzoate

Conditions

Conditions	Yield
With potassium carbonate In acetone at 65℃; for 20h;	100%
With potassium carbonate In dimethyl sulfoxide at 20℃; for 8h;	99%
With potassium carbonate In acetone Heating;	89%

: 121-44-8
triethylamine

: 106-95-6
allyl bromide

: 29443-23-0
N,N,N-triethylprop-2-en-1-aminium bromide

Conditions

Conditions	Yield
In ethanol at 95℃; for 48h;	100%
for 2h; Reflux;	92%

: 119-61-9
benzophenone

: 106-95-6
allyl bromide

: 4165-79-1
1,1-diphenyl-3-buten-1-ol

Conditions

Conditions	Yield
With ammonium acetate; zinc In tetrahydrofuran at 0℃; for 0.0166667h; Barbier reaction;	100%
With manganese; chloro-trimethyl-silane; indium In tetrahydrofuran at 20℃; for 4h; Alkylation;	98%
With manganese; chloro-trimethyl-silane; indium In tetrahydrofuran at 20℃; for 4h; Barbier allylation;	98%

: 111-71-7
heptanal

: 106-95-6
allyl bromide

: 36971-14-9
dec-1-en-4-ol

Conditions

Conditions	Yield
With ammonium chloride; zinc In tetrahydrofuran for 1h; Ambient temperature;	100%
With silica gel; ammonium chloride; zinc for 16h; Product distribution; Mechanism; Ambient temperature; other carbonyl compounds; other allyl halides; var. solid or liquid phases; var. reaction time;	98%
With chloro-trimethyl-silane; Piperonyl butoxide; tetrabutylammomium bromide In N,N-dimethyl-formamide for 2h; Ambient temperature;	98%

: 106-41-2
4-bromo-phenol

: 106-95-6
allyl bromide

: 25244-30-8
4-(allyloxy)bromobenzene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 16h; Alkylation;	100%
With potassium carbonate In N,N-dimethyl-formamide at 60℃;	99%
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 0.833333h;	99%

: 116-17-6
triisopropyl phosphite

: 106-95-6
allyl bromide

: 1067-70-5
Diisopropyl allylphosphonate

Conditions

Conditions	Yield
With 2,6-di-tert-butyl-4-methyl-phenol at 115℃; for 16h;	100%
for 16h; Heating;	95%

: 90-15-3
α-naphthol

: 106-95-6
allyl bromide

: 20009-25-0
allyl naphthyl ether

Conditions

Conditions	Yield
With potassium carbonate In acetone at 20℃; Reflux;	100%
With tetra-(n-butyl)ammonium iodide; potassium carbonate In acetone for 1h; Reflux; Inert atmosphere;	100%
With potassium carbonate In N,N-dimethyl-formamide at 20℃;	99%

: 533-58-4
2-Iodophenol

: 106-95-6
allyl bromide

: 24892-63-5
1-allyloxy-2-iodobenzene

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide	100%
With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 24h;	99%
With potassium carbonate In N,N-dimethyl-formamide at 60℃; for 2h; Inert atmosphere;	99%

: 93-51-6
2-Methoxy-4-methylphenol

: 106-95-6
allyl bromide

: 201359-55-9
1-(allyloxy)-2-methoxy-4-methylbenzene

Conditions

Conditions	Yield
With potassium carbonate In acetone for 12h; Heating;	100%
With potassium carbonate; sodium iodide In acetone for 15h; Reflux; Inert atmosphere;	96%
With potassium carbonate In acetone for 6h; Heating;	95%

: 529-35-1
5,6,7,8-Tetrahydronaphthalen-1-ol

: 106-95-6
allyl bromide

: 107203-35-0
5-(allyloxy)-1,2,3,4-tetrahydronaphthalene

Conditions

Conditions	Yield
With caesium carbonate In N,N-dimethyl-formamide at 25℃; for 2h; Inert atmosphere;	100%
With methanol; sodium methylate
With sodium; toluene at 70 - 80℃;
With potassium carbonate; acetone

: 3251-56-7
2-methoxy-4-nitrophenol

: 106-95-6
allyl bromide

: 99060-58-9
1-(allyloxy)-2-methoxy-4-nitrobenzene

Conditions

Conditions	Yield
With potassium carbonate In acetone at 55℃; for 12h;	100%
With potassium carbonate; acetone
at 70℃; for 6h;

: 540-38-5
4-Iodophenol

: 106-95-6
allyl bromide

: 13997-71-2
1-(allyloxy)-4-iodobenzene

Conditions

Conditions	Yield
With tetrabutylammomium bromide; sodium hydroxide In 2-methyltetrahydrofuran; water for 0.5h; Reflux;	100%
With potassium carbonate In acetone for 1h; Reflux;	98%
Stage #1: allyl bromide With sodium hydride In N,N-dimethyl-formamide; oil at -10℃; for 0.166667h; Stage #2: p-Iodophenol In N,N-dimethyl-formamide; oil for 0.75h;	96%

: 95-56-7
2-hydroxybromobenzene

: 106-95-6
allyl bromide

: 60333-75-7
O-allyl-2-bromophenol

Conditions

Conditions	Yield
With potassium carbonate In acetone for 6h; Heating / reflux;	100%
With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.5h;	99%
With potassium carbonate In N,N-dimethyl-formamide at 60℃; Schlenk technique;	99%

: 90-44-8
anthracen-9(10H)-one

: 106-95-6
allyl bromide

: 57996-28-8
10,10-bisallylanthrone

Conditions

Conditions	Yield
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane for 1.5h; Ambient temperature;	100%
With sodium hydroxide In water for 2h;	70%
With N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide In dichloromethane; water for 1h; Schlenk technique; Inert atmosphere;	63%
With lithium methanolate

: 13319-71-6
2-bromo-6-methylphenol

: 106-95-6
allyl bromide

: 854260-75-6
2-(allyloxy)-1-bromo-3-methylbenzene

Conditions

Conditions	Yield
Stage #1: 2-bromo-6-methylphenol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.0833333h; Stage #2: allyl bromide In N,N-dimethyl-formamide; mineral oil at 20℃;	100%
With potassium carbonate; acetone
Stage #1: 2-bromo-6-methylphenol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; Stage #2: allyl bromide In N,N-dimethyl-formamide; mineral oil at 0 - 25℃; Stage #3: With water In N,N-dimethyl-formamide; mineral oil

: 121-71-1
3-Hydroxyacetophenone

: 106-95-6
allyl bromide

: 58621-54-8
1-(3-(allyloxy)phenyl)ethanone

Conditions

Conditions	Yield
With potassium carbonate In acetone at 20℃; Reflux;	100%
With potassium carbonate In acetone for 8h; Heating;	95%
With potassium carbonate In ethanol for 3h; Reflux; Inert atmosphere;	93%