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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096150Generated: October 31, 2026

t-Butyl bromide → Tert-butyl 4-cyano-5-(methylthio)thiophene-2-carboxylate

https://huagongshe.com/reaction/1096150

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyl bromideHCID 10485—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Cyano-5-methylsulfanylthiophene-2-carboxylic acidHCID 45594312—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductTert-butyl 4-cyano-5-(methylthio)thiophene-2-carboxylateHCID 6678590058.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-cyano-5-(methylthio)thiophene-2-carboxylic acid (2.0 g, 10 mmol), benzyltrimethylammonium chloride (2.25 g, 10 mmol), tertbutyl bromide (54 mL, 480 mmol) and anhydrous potassium carbonate (36 g, 260 mmol) in dimethylacetamide (100 mL) was stirred at 60° C. for 6 hours. After cooling, the mixture was diluted with ethyl acetate (400 mL) and washed with water. Organic layer was dried and evaporated under reduced pressure to give a residue which was purified by chromatography (eluent ethyl acetate/n-hexane 3:1) thus yielding 1.5 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138217B2
Source datasetuspto-grants-2012_03
ORD IDord-cc1cac696e15496f92665e781843175e
Source noteuspto-grants-2012_03