Dayangchem's R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. DayangChem can provide different quantities
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inquiryName: 3-Methyl-1-butene Other Names: Methylbutene; 3-Methylbutene; 3-methylbut-1-ene; isopentene; Isoamylene; 3-Methylbutene-1 CAS: 563-45-1 MF: C5H10 Appearance: Colorless Transparent Liquid Storage: Preserve in well-closed, light-resist
suoerior quality moderate price & quick delivery Appearance:A colorless volatile liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryAmoychem is committed to providing the top-quality chemical products and services Internationally. We offer our customers with friendly, professional service and reliable, high performance products that have been manufactured according to the accredi
BaiFuChem is a Professional chemical raw material supplier in China, our main products include Biochemical , Pharma Intermediate and Organic chemical etc. BaiFuChem have wealth of products,experience , expertise and state-of-the-art
Aopharm is specialized in APIs, pharmaceutical intermediates & fine chemicals. 1. The best quality, competitive price. 2. The best service before or after shipment. 3. Rich experience in export operation. 4. Rich experience in modes of tran
3-Methyl 1-Butene supplierAppearance:crystalline white powder Storage:Keep away of light,cool place Package:25kg/drum;200kg/drum Application:Pharma Intermediate Transportation:Sea/air/courier
With about ten years experiences in the field of pharmaceutical chemicals, Yierdechem has established solid business cooperation relationships with many large companys worldwide.As a leading supplier of API and pharmaceutical intermediates, holds its
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Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio
Gas-phase reaction of the OH radical with 3-methyl-1-butene in the presence of NO has been investigated. Polymerization of 3-methyl-1-butene in the presence of homogeneous metallocene catalyst (co-catalyst methylalumoxane) has been investigated. Pack
(E)-trimethyl-(β-methylcrotyl)silane
3-Methyl-1-butene
Conditions | Yield |
---|---|
With tetrahydrofuran at 60℃; for 3h; Heating; | 100% |
WCl2(PMePh2)4
ethene
A
WCl2{P(CH3)(C6H5)2}2(O)(C2H4)
B
3-Methyl-1-butene
Conditions | Yield |
---|---|
With acetone In benzene-d6 2 mol equiv. acetone and 2 mol equiv. C2H4 condensed into NMR tube contg. 1 mol equiv. soln. W-complex/C6D6 at -196°C, tube sealed; not isolated, detected by NMR-spect.; other uncharacterized products also present; | A 94% B 31% |
Conditions | Yield |
---|---|
Ba-compounds on Al2O3 at 340℃; Product distribution / selectivity; Gas phase; | A 7% B 91.1% |
aluminium oxide SP 537 at 280℃; under 1125.11 Torr; Product distribution / selectivity; | |
With aluminum oxide at 250 - 325℃; Temperature; | |
With aluminum oxide at 325℃; Flow reactor; | A 10 %Chromat. B 86.2 %Chromat. |
2-Methylbutyraldehyde
isoprene
A
3-methyl-butan-2-one
B
2-methyl-but-2-ene
C
3-Methyl-1-butene
D
pivalaldehyde
Conditions | Yield |
---|---|
With steam; calcium phosphate catalyst TU 103-134-72 at 380℃; Product distribution; Rate constant; Kinetics; other conditions - var. space velocity of adding reagent, var. dilution with steam, var. temp., var. contact time, other object - activation energy data;; | A 8.2% B n/a C n/a D 0.6% E n/a |
(E)-trimethyl-(β-methylcrotyl)silane
A
2-methyl-but-2-ene
B
3-Methyl-1-butene
Conditions | Yield |
---|---|
With potassium tert-butylate In N,N,N,N,N,N-hexamethylphosphoric triamide at 60℃; for 3h; | A 85% B 5% |
(4S)-4-isopropyl-2-phenyl-4,5-dihydro-1λ6,3-thiazole 1,1-dioxide
A
3-Methyl-1-butene
B
benzonitrile
Conditions | Yield |
---|---|
at 600℃; under 0.001 Torr; | A 68% B 83% |
A
2,2-dimethylpropane
B
ethene
C
1,1-dimethylcyclopropane
D
3-Methyl-1-butene
E
isobutene
Conditions | Yield |
---|---|
In toluene inert atmosphere, thermal decompn. (85°C); GLC; | A 5% B 5% C 74% D 4% E 12% |
triethylbenzylammonium ethanolate
i-pentyl bromide
A
1-ethoxy-3-methyl-butane
B
3-Methyl-1-butene
Conditions | Yield |
---|---|
at 20 - 25℃; for 1h; | A 62% B 2.2% |
Dimethylallene
A
2-methyl-but-2-ene
B
methylbutane
C
2-Methyl-1-butene
D
3-Methyl-1-butene
Conditions | Yield |
---|---|
With hydrogen; palladium dichloride In N,N-dimethyl-formamide under 18751.5 Torr; for 0.133333h; Product distribution; Ambient temperature; various time; | A 57.5% B 1.2% C 0.1% D 25.2% |
2-chloro-3-methyl-butan-1-ol
3-Methyl-1-butene
Conditions | Yield |
---|---|
With n-butyllithium; naphthalen-1-yl-lithium at -100℃; | 54% |
A
2,2-dimethylpropane
B
ethene
C
1,1-dimethylcyclopropane
D
3-Methyl-1-butene
E
isobutene
Conditions | Yield |
---|---|
With triphenylphosphine In toluene inert atmosphere, thermal decompn. (24°C, 5-fold molar excess PPh3); GLC; | A 2% B 28% C 11% D 7% E 52% |
In toluene inert atmosphere, thermal decompn. (24°C); GLC; | A 6% B 15% C 47% D 6% E 26% |
A
2,2-dimethylpropane
B
ethene
C
1,1-dimethylcyclopropane
D
3-Methyl-1-butene
E
isobutene
Conditions | Yield |
---|---|
In toluene inert atmosphere, thermal decompn. (60°C); GLC; | A 5% B 14% C 51% D 3% E 27% |
Conditions | Yield |
---|---|
With triethylbenzylammonium ethanolate at 20 - 25℃; for 1h; | A 50% B 19.8% |
ethanol
A
1-(dimethylphenylsilyl)-3-methyl-2-butene
B
3-(dimethylphenylsilyl)-1,1-dimethyl-1-propanol
C
4-(dimethylphenylsilyl)-2-methyl-1-butene
D
3-Methyl-1-butene
Conditions | Yield |
---|---|
In water at 50℃; Rate constant; | A 49% B 24% C 12% D 3% E 12% |
2,2,2-trifluoroethanol
A
1-(dimethylphenylsilyl)-3-methyl-2-butene
B
3-(dimethylphenylsilyl)-1,1-dimethyl-1-propanol
C
4-(dimethylphenylsilyl)-2-methyl-1-butene
D
3-Methyl-1-butene
Conditions | Yield |
---|---|
In water at 50℃; Rate constant; | A 47% B 8% C 7% D 18% E 20% |
cyclopentadienylirondicarbonyl hydride
isoprene
A
2-methyl-but-2-ene
B
cyclopentadienyl iron(II) dicarbonyl dimer
C
(η5-cyclopentadienyl)Fe(CO)2(CH2CH=C(CH3)2)
D
2-Methyl-1-butene
E
3-Methyl-1-butene
Conditions | Yield |
---|---|
In pentane under N2, stirring at room temp, the react. was complete within 20-30 min; evapn. (vac.), chromy. on alumina (eluent pentane for the hydrometalated products, and more polar solvents for the dimer), the org. products identiefied by GC and NMR; | A n/a B 46% C 19% D n/a E n/a |
(Z)-pent-2-ene
A
methane
B
butene-2
C
ethane
D
1-penten
E
3-Methyl-1-butene
F
buta-1,3-diene
Conditions | Yield |
---|---|
hydrogen sulfide at 469.9℃; Rate constant; Kinetics; Product distribution; mechanism; effects of temperature, concentration; further products; | A 43.3% B 2.9% C 1.6% D 4.5% E 0.5% F 39.5% |
Conditions | Yield |
---|---|
With hydrogen; potassium; magnesium oxide at 99.9℃; | A 8.8% B 41.2% |
With tri-1-napthylphosphine; hydrogen In dichloromethane-d2 at 50℃; under 3750.38 Torr; for 240h; Glovebox; Inert atmosphere; Sealed tube; | A 82 %Spectr. B 8 %Spectr. |
Methylenetriphenylphosphorane
3-Methyl-1-butene
Conditions | Yield |
---|---|
for 24h; Ambient temperature; | 40% |
isoprene
A
2-methyl-but-2-ene
B
methylbutane
C
2-Methyl-1-butene
D
3-Methyl-1-butene
Conditions | Yield |
---|---|
With hydrogen; palladium dichloride In N,N-dimethyl-formamide under 18751.5 Torr; for 0.116667h; Product distribution; Ambient temperature; various time; | A 38.5% B 0.8% C 20.5% D 22% |
With hydrogen; Pd2Cl2<<(EtO)2PO>2H>2 In ethanol at 20℃; Product distribution; influence of reaction time on pruduct distribution; | |
With hydrogen Product distribution; Rate constant; various Ni-catalysts (Ni-P, Ni-B, Raney nickel), temperatures; |
2-isopropyl-5-methyl-2,3-dihydro-thiophene
dimethyl acetylenedicarboxylate
A
5-methyl-thiophene-2,3-dicarboxylic acid dimethyl ester
B
3-Methyl-1-butene
Conditions | Yield |
---|---|
In benzene at 80℃; | A 37% B n/a |
methylbutane
A
2-methyl-but-2-ene
B
penta-1,3-diene
C
cyclopenta-1,3-diene
D
2-Methyl-1-butene
E
3-Methyl-1-butene
F
pentane
G
isoprene
Conditions | Yield |
---|---|
With platinum-aluminum catalyst at 600℃; Gas phase; | A n/a B n/a C n/a D n/a E n/a F n/a G 28.72% |
isobutene
A
1-butylene
B
(Z)-2-Butene
C
2-methyl-but-2-ene
D
Z-piperylene
E
1-methylbuta-1,3-diene
F
propene
G
methane
H
trans-2-Butene
I
(Z)-pent-2-ene
J
(E)-pent-2-ene
K
ethane
L
propane
M
Isobutane
N
methylbutane
O
ethene
P
1-penten
Q
Cyclopentane
R
2-Methyl-1-butene
S
3-Methyl-1-butene
T
cyclopentene
U
n-butane
V
pentane
Conditions | Yield |
---|---|
CBV1502 at 579.84℃; under 900.09 Torr; Product distribution / selectivity; | A 2.6% B 2.4% C 1.29% D 0.05% E 0.03% F 24.95% G 0.73% H 3.19% I 0.32% J 0.58% K 0.36% L 2.08% M 2.15% N 0.34% O 9.61% P 0.23% Q 0.4% R 0.71% S 0.14% T 0.14% U 1.8% V 0.16% |
CBV28014 at 509.84℃; under 900.09 Torr; Product distribution / selectivity; | A 6.71% B 7.3% C 5.62% D 0.02% E 0.03% F 23.29% G 0.09% H 9.97% I 1.1% J 2.06% K 0.07% L 1.24% M 1.95% N 0.59% O 3.25% P 0.7% Q 0.31% R 2.72% S 0.47% T 0.21% U 1.37% V 0.26% |
isoprene
A
2-methyl-but-2-ene
B
2-Methyl-1-butene
C
3-Methyl-1-butene
Conditions | Yield |
---|---|
With hydrogen; 1-n-butyl-3-methylimidazolium hexafluoroantimonate; [(bis(diphenylphosphino)ethane)Rh(norbornadiene)][PF6] | A 23% B 22% C 10% |
With hydrogen; potassium cyanide; potassium hydroxide; potassium chloride; β‐cyclodextrin; cobalt(II) chloride In benzene under 760 Torr; for 10h; Ambient temperature; Yield given. Yields of byproduct given; | |
With sodium tetrahydroborate; complex of Pd with (C2H5O)2P(O)Cl In ethanol at 20℃; for 0.0666667h; Yield given; |
A
1,3-dibenzylurea
B
N-benzylidene benzylamine
C
3-Methyl-1-butene
D
benzonitrile
E
1,1'-(1,2-ethanediyl)bisbenzene
F
isobutyraldehyde
Conditions | Yield |
---|---|
at 650℃; under 0.001 - 0.002 Torr; for 2.77778E-06h; Product distribution; other products of flash vacuum pyrolysis; | A 10% B 7% C 12% D 16% E 6% F 5% |
Conditions | Yield |
---|---|
at 750℃; under 0.007 Torr; | 15% |
at 500℃; | |
at 600℃; | |
at 700℃; im Stickstoffstrom an Glaswolle; | |
at 500℃; Pyrolysis; |
propene
A
1,4-Pentadiene
B
methane
C
propane
D
1-penten
E
3-Methyl-1-butene
F
cyclopropane
Conditions | Yield |
---|---|
at -78.1℃; Product distribution; excited by the impact of low-energy electrons; | A 0.12% B 0.57% C 0.99% D 0.094% E 0.032% F 0.21% |
diethyl sulfate
isopentyl ether
A
(+-)-5-methyl-3-hexanol
B
3-Methyl-1-butene
Conditions | Yield |
---|---|
at 195℃; |
Conditions | Yield |
---|---|
With aluminum oxide | |
at 250 - 400℃; an Al2O3 oder Al2O3-Mischkatalysatoren; |
2-methyl-but-2-ene
A
1-penten
B
2-Methyl-1-butene
C
3-Methyl-1-butene
D
2-pentene
Conditions | Yield |
---|---|
at 200 - 380℃; Gleichgewichtsbestimmungen bei der Umlagerung ueber Silicagel; |
tetrafluoroboric acid diethyl ether
3-Methyl-1-butene
Conditions | Yield |
---|---|
With C6H5Cl In chlorobenzene addn. of HBF4*Et2O to mixt. of the rhenium complex and C6H5Cl (under N2, -45°C, with stirring, 15 min), addn. of excess 3-methyl-but-1-ene, after 30 min cold bath removed, stirred (20 h); mixt. filtered into hexane, ppt. collected, washed with pentane, dried in vac.; 2 diastereomers: (RS,SR)/(RR,SS) = 62:38; | 99% |
With CH2Cl2 In dichloromethane addn. of HBF4*Et2O to mixt. of the rhenium complex and CH2Cl2 (NMR tube, under N2, -80°C, shaken), addn. of 3-methyl-but-1-ene at -78°C, allowed to warm to 20°C, kept at room temp. (2 d); mixt. filtered, addn. of hexane to the filtrate, ppt. collected, chromy. (silica gel, acetone/CH2Cl2); elem. anal.; 2 diastereomers: (RS,SR)/(RR,SS) = 67:33; | 59% |
[(C5(CH3)5)2Y(CH(CH3)CH2CH3)]
3-Methyl-1-butene
[(C5(CH3)5)2Y(CH2CH2CH(CH3)2)]
Conditions | Yield |
---|---|
In not given byproducts: 2-butene; at -60°C; | 99% |
3-Methyl-1-butene
[(C5(CH3)5)2Y(CH2CH2CH(CH3)2)]
Conditions | Yield |
---|---|
In further solvent(s) 1:1 methylcyclohexane-d14 : pentane-d12, -78°C, few min; not sepd., detected by NMR spectra; | 99% |
3-Methyl-1-butene
1,2-dibromo-3-methylbutane
Conditions | Yield |
---|---|
With bromine In chloroform at -65℃; | 95% |
With bromine In dichloromethane for 1h; | 86.9% |
With bromine |
ethyl 5,7-dimethoxy-2-oxo-2H-chromene-3-carboxylate
3-Methyl-1-butene
Conditions | Yield |
---|---|
In benzene Irradiation; | 94% |
3-Methyl-1-butene
(3R,4R)-5-(tert-butyldimethylsiloxy)-3,4-(isopropylidenedioxy)pent-1-ene
tert-Butyl-[(4R,5R)-2,2-dimethyl-5-((E)-3-methyl-but-1-enyl)-[1,3]dioxolan-4-ylmethoxy]-dimethyl-silane
Conditions | Yield |
---|---|
tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In dichloromethane at 40℃; for 38h; | 94% |
Conditions | Yield |
---|---|
In toluene byproducts: LiCl; NaAlH4 loaded in a vertical-type ball mill under Ar or N2; toluene added; mixt. agitated for 10 min at 70°C; mixt. of Et22AlCl with olefin (NaAlH4:Et2AlCl:olefin=1.04:1.0:4.5) added; mixt. agitated for 1.5 h at 100°C; cooled; suspn. filtered off under Ar; solvent and olefin removed (vac.);elem. anal.; | 93% |
Conditions | Yield |
---|---|
Stage #1: 3-Methyl-1-butene With copper(l) iodide; Schwartz's reagent; (3,5-dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)-bis-(1-phenyl-ethyl)-amine In dichloromethane; chloroform at 20℃; for 0.4h; Stage #2: 3-chloro-cyclohexene In dichloromethane; chloroform | 93% |
diethylaluminium chloride
3-Methyl-1-butene
isoamylethylaluminum hydride
Conditions | Yield |
---|---|
In toluene byproducts: LiCl; NaAlH4 loaded in a vertical-type ball mill under Ar or N2; toluene added; mixt. agitated for 10 min at 70°C; mixt. of Et22AlCl with olefin (NaAlH4:Et2AlCl:olefin=1.04:1.0:1.98) added; mixt. agitated for 1.5 h at 100°C; cooled; suspn. filtered off under Ar; solvent and olefin removed (vac.);elem. anal.; | 92.2% |
carbon monoxide
3-Methyl-1-butene
A
(2s)-(+)-2,3-dimethyl-1-butanal
B
(R)-2,3-dimethylbutanal
C
isocaproic aldehyde
Conditions | Yield |
---|---|
With acetylacetonatodicarbonylrhodium(l); hydrogen; (R,S)-binaphos In benzene under 76000 Torr; Yields of byproduct given; | A n/a B n/a C 92% |
With acetylacetonatodicarbonylrhodium(l); hydrogen; (R,S)-binaphos In benzene under 76000 Torr; Yield given. Yields of byproduct given. Title compound not separated from byproducts; | A n/a B n/a C 92% |
3-Methyl-1-butene
2-chloro-3-methyl-1-(pentafluoro-λ6-sulfanyl)butane
Conditions | Yield |
---|---|
Stage #1: 3-Methyl-1-butene With pentafluorosulfanyl chloride In dichloromethane at -40℃; Stage #2: With triethyl borane In hexane; dichloromethane at -40 - 20℃; Stage #3: With water; sodium hydrogencarbonate In hexane; dichloromethane | 92% |
piperidine
3-Methyl-1-butene
phenylacetylene
4-(1-isopropyl-3-phenyl-2-propynyl)piperidine
Conditions | Yield |
---|---|
With polystyrene supported 1,2,3-triazolyl N-methylimidazolyl silver bromide complex In dichloromethane at 20℃; for 12h; Schlenk technique; | 92% |
Conditions | Yield |
---|---|
With tin(IV) chloride In dichloromethane at -60℃; for 0.0833333h; | 91% |
3-benzyloxycarbonyl-5,7-dimethoxycoumarin
3-Methyl-1-butene
Conditions | Yield |
---|---|
In benzene for 24h; Irradiation; | 91% |
(2S,3R,4S,5R)-2,3,4,5-tetra(benzyloxy)-N-((S)-2-oxoazepa-3-yl)hept-6-enamide
3-Methyl-1-butene
(2S,3R,4S,5R,E)-2,3,4,5-tetra(benzyloxy)-8-methyl-N-((S)-2-oxoazepan-3-yl)non-6-enamide
Conditions | Yield |
---|---|
With Hoveyda-Grubbs catalyst second generation In dichloromethane for 24h; Reflux; | 90% |
(2R,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-3-((4S,5R)-2,2-dimethyl-5-vinyl-[1,3]dioxolan-4-yl)-2-methoxy-N-((S)-2-oxo-azepan-3-yl)-propionamide
3-Methyl-1-butene
Conditions | Yield |
---|---|
[1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(O-isopropoxyphenylmethylene)ruthenium In dichloromethane at 40℃; | 89% |
(2R,3R,4S,5R)-2,3,4,5-tetra(benzyloxy)-N-((S)-2-oxoazepan-3-yl)hept-6-enamide
3-Methyl-1-butene
(2R,3R,4S,5R,E)-2,3,4,5-tetra(benzyloxy)-8-methyl-N-((S)-2-oxoazepan-3-yl)non-6-enamide
Conditions | Yield |
---|---|
With Hoveyda-Grubbs catalyst second generation In dichloromethane for 24h; Reflux; | 89% |
tert-butyl 5,7-dimethoxycoumarin-3-carboxylate
3-Methyl-1-butene
Conditions | Yield |
---|---|
In benzene for 24h; Irradiation; | 88% |
(2S,3R,4S,5R)-3,4,5-tris(benzyloxy)-2-methoxy-N-((S)-2-oxoazepan-3-yl)hept-6-enamide
3-Methyl-1-butene
(2S,3R,4S,5R,E)-3,4,5-tris(benzyloxy)-2-methoxy-8-methyl-N-((S)-2-oxoazepan-3-yl)non-6-enamide
Conditions | Yield |
---|---|
With Hoveyda-Grubbs catalyst second generation In dichloromethane for 24h; Reflux; | 88% |
(2R,3S,4R)-2,3,4-tris(benzyloxy)-N-((S)-2-oxoazepan-3-yl)hex-5-enamide
3-Methyl-1-butene
(2R,3S,4R,E)-2,3,4-tris(benzyloxy)-7-methyl-N-((S)-2-oxoazepan-3-yl)oct-5-enamide
Conditions | Yield |
---|---|
With Hoveyda-Grubbs catalyst second generation In dichloromethane for 24h; Reflux; | 88% |
(2S,3S,4R)-2,3,4-tris(benzyloxy)-N-((S)-2-oxoazepan-3-yl)hex-5-enamide
3-Methyl-1-butene
(2S,3S,4R,E)-2,3,4-tris(benzyloxy)-7-methyl-N-((S)-2-oxoazepan-3-yl)oct-5-enamide
Conditions | Yield |
---|---|
With Hoveyda-Grubbs catalyst second generation In dichloromethane for 24h; Reflux; | 88% |
3-Methyl-1-butene
Conditions | Yield |
---|---|
With sodium chlorite; sodium dihydrogenphosphate In tetrahydrofuran; tert-butyl alcohol at 0℃; for 0.25h; | 88% |
3-Methyl-1-butene
α-bromoacetophenone
2-(3-methylbut-2-enylsulfonyl)-1-phenylethanone
Conditions | Yield |
---|---|
Stage #1: 3-Methyl-1-butene With sulfur dioxide; boron trichloride In dichloromethane at -196 - -20℃; for 3h; Stage #2: With sodium hydroxide In dichloromethane at 5 - 20℃; Stage #3: α-bromoacetophenone With tetrabutyl-ammonium chloride In dichloromethane at 20℃; for 12h; | 87% |
3-Methyl-1-butene
N-sulfinyl-p-toluenesulfonamide
N-(3-Methyl-2-butenylsulfinyl)-p-toluolsulfonamid
Conditions | Yield |
---|---|
In toluene at 20℃; for 18h; | 85% |
1,1,1,3,3,3-hexafluoroisopropyl iodide
3-Methyl-1-butene
1,1,1-Trifluoro-4-iodo-5-methyl-2-(trifluoromethyl)hexane
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) at 80℃; for 10h; | 84% |
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