Thiophene-2-acetic acid
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
With bis(trichloromethyl) carbonate; N,N-dimethyl-formamide In dichloromethane at -10 - 0℃; for 5h; Temperature; Reagent/catalyst; | 94.7% |
With phosgene; 4-cyclopentylaminopyridine hydrobromide In toluene | 92% |
With 1-butyl-3-methylimidazolium hydroxide; thionyl chloride In chloroform at 10℃; for 8h; Reagent/catalyst; Temperature; | 89.8% |
Conditions | Yield |
---|---|
With thionyl chloride; triethylamine In chloroform; water; ethyl acetate | A n/a B 84% |
2-Thiophenecarbonyl chloride
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: diethyl ether / 0 °C 2: aq. Ag2O / dioxane 3: (COCl)2; DMF / CH2Cl2 View Scheme |
2-thiophenylcarboxylic acid
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: (COCl)2; DMF / CH2Cl2 2: diethyl ether / 0 °C 3: aq. Ag2O / dioxane 4: (COCl)2; DMF / CH2Cl2 View Scheme |
2-diazo-1-(thiophen-2-yl)ethanone
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq. Ag2O / dioxane 2: (COCl)2; DMF / CH2Cl2 View Scheme |
2-Chloromethylthiophene
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: acetone; water 2: aq.-ethanolic KOH-solution 3: thionyl chloride View Scheme | |
Multi-step reaction with 3 steps 1: acetone; water 2: aq.-ethanolic KOH-solution 3: thionyl chloride View Scheme |
2-cyanomethylthiophene
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: aq.-ethanolic KOH-solution 2: thionyl chloride View Scheme |
Conditions | Yield |
---|---|
With thionyl chloride; triethylamine In dichloromethane | |
With thionyl chloride; triethylamine In dichloromethane |
isopropyl 2-(thiophen-2-yl)acetate
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogenchloride / water; acetonitrile / 10 h / Reflux 2: pyridine; thionyl chloride / dichloromethane / 1 h / Reflux View Scheme |
ethyl thiophen-2-ylacetate
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogenchloride / ethanol; water / 8 h / Reflux 2: pyridine; thionyl chloride / dichloromethane / 1 h / Reflux View Scheme |
methyl 2-thiopheneacetate
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: hydrogenchloride / water; acetonitrile / 8 h / Reflux 2: pyridine; thionyl chloride / dichloromethane / 1 h / Reflux View Scheme |
Conditions | Yield |
---|---|
at 20℃; for 4h; | 100% |
for 0.5h; | 82% |
at 20℃; for 3h; |
2-thienylacetic acid chloride
phosphorous acid trimethyl ester
(2-Thiophen-2-yl-acetyl)-phosphonic acid dimethyl ester
Conditions | Yield |
---|---|
In diethyl ether Ambient temperature; | 100% |
at 0 - 20℃; for 3h; | 88% |
In tetrahydrofuran Heating; | |
at 0℃; for 1h; Reflux; |
2-thienylacetic acid chloride
2-(trifluoromethyl)benzenamine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 100% |
2-thienylacetic acid chloride
3-nitro-aniline
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 100% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 100% |
2-thienylacetic acid chloride
2-{[(2-biphenyl-4-yl-(1S)-methoxycarbonyl-ethyl)-(4'-trifluoromethyl-biphenyl-4-carbonyl)-amino]-methyl}-(2R)-pyrrolidinium chloride
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; for 1h; | 100% |
2-thienylacetic acid chloride
C16H14N4OS
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 100% |
2-thienylacetic acid chloride
ethyl (S)-1-(2-thiopheneacetyl)-3-piperidinecarboxylate
Conditions | Yield |
---|---|
With sodium carbonate In water; ethyl acetate at 20℃; for 0.5h; Schotten-Baumann Reaction; Green chemistry; | 100% |
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 98% |
2-thienylacetic acid chloride
{3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}amine
N-{3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}-2-(2-thienyl)acetamide
Conditions | Yield |
---|---|
Stage #1: 2-thienylacetic acid chloride; {3-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]phenyl}amine With triethylamine In tetrahydrofuran Stage #2: With PS-Trisamine In tetrahydrofuran for 16h; | 98% |
2-thienylacetic acid chloride
ethylenediamine
N,N'-di(2-thiopheneacetyl)ethylenediamine
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 97% |
2-thienylacetic acid chloride
5-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]-2-methylaniline
N-{5-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]-2-methylphenyl}-2-(2-thienyl)acetamide
Conditions | Yield |
---|---|
Stage #1: 2-thienylacetic acid chloride; 5-[3-(2-chloro-4-pyrimidinyl)pyrazolo[1,5-a]pyridin-2-yl]-2-methylaniline With PS-Trisamine In tetrahydrofuran for 16h; Stage #2: With triethylamine In tetrahydrofuran | 97% |
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide; hydroquinone; ammonium perrhenate In ethyl acetate for 0.5h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 96% |
2-thienylacetic acid chloride
aniline
N-phenyl-2-(thiophen-2-yl)acetamide
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; | 96% |
2-thienylacetic acid chloride
Conditions | Yield |
---|---|
In acetonitrile at 23℃; for 2h; Inert atmosphere; | 96% |
2-thienylacetic acid chloride
methyl 2-amino-5-methylthiophene-3-carboxylate
Conditions | Yield |
---|---|
In 1,4-dioxane at 98℃; | 95.5% |
2-thienylacetic acid chloride
9-Methyl-5-thia-6,13-diaza-benzo[4,5]cyclohepta[1,2-b]naphthalene
C23H16N2OS2
Conditions | Yield |
---|---|
With triethylamine In benzene for 1h; Heating; | 95% |
2-thienylacetic acid chloride
3-[3-(2-chloro-4-pyrimidinyl)-4-fluoropyrazolo[1,5-a]pyridin-2-yl]aniline
N-{3-[3-(2-chloro-4-pyrimidinyl)-4-fluoropyrazolo[1,5-a]pyridin-2-yl]phenyl}-2-(2-thienyl)acetamide
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 0.5h; | 95% |
2-thienylacetic acid chloride
2-(1-cyclohexenyl)ethylamine
N-<2-(cyclohexen-1-yl)ethyl>thiophene-2-acetamide
Conditions | Yield |
---|---|
With potassium carbonate In benzene for 1h; Ambient temperature; | 94% |
2-thienylacetic acid chloride
3-amino-5-bromobenzoic acid methyl ester
methyl 3-bromo-5-[2-(thiophen-2-yl)acetamido]benzoate
Conditions | Yield |
---|---|
In N,N-dimethyl acetamide at 20℃; Inert atmosphere; Cooling with ice; | 94% |
2-thienylacetic acid chloride
berberrubine chloride
C25H20NO5S(1+)*Cl(1-)
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 0.5h; | 94% |
2-thienylacetic acid chloride
(S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride
Conditions | Yield |
---|---|
Stage #1: (S)-(-)-(5-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)propylamine hydrochloride With sodium carbonate In dichloromethane; water at 27℃; for 1h; Stage #2: 2-thienylacetic acid chloride In dichloromethane; water at 27℃; for 1h; | 94% |
2-thienylacetic acid chloride
quino<2,3-b><1,5>benzoxazepine
C22H14N2O2S
Conditions | Yield |
---|---|
With triethylamine In benzene for 1h; Heating; | 93% |
2-thienylacetic acid chloride
quino<2,3-b><1,5>benzothiazepine
C22H14N2OS2
Conditions | Yield |
---|---|
With triethylamine In benzene for 1h; Heating; | 93% |
Accidental Release Measures of 2-Thiopheneacetyl chloride(39098-97-0)
【Small spills/leaks】Clean up spills immediately, using the appropriate protective equipment. Absorb spill using an absorbent, non-combustible material such as earth, sand, or vermiculite. Provide ventilation. Do not get water inside containers.
Stability and Reactivity of 2-Thiopheneacetyl chloride(39098-97-0)
【Stability】Stable under normal temperatures and pressures. May decompose on exposure to moist air or water. Moisture sensitive.
【Incompatibilities】Strong oxidizing agents, strong bases, moisture.
【Decomposition】Hydrogen chloride, carbon monoxide, oxides of sulfur, carbon dioxide.
【Combustion Products】Fire may produce irritating, corrosive and/or toxic gases.
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