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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63300Generated: October 27, 2026

Potassium Carbonate → Cyclohexylmethyl 5-chlorothiophene-2-carboxylate

https://huagongshe.com/reaction/63300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloro-2-thiophenecarboxylic acidHCID 95048—
ReactantCyclohexane, (bromomethyl)-HCID 137636—
SolventWaterHCID 962—
ProductCyclohexylmethyl 5-chlorothiophene-2-carboxylateHCID 84819867—

Reaction Steps

A mixture of 5-chlorothiophene-2-carboxylic acid (3.01 g, 19.0 mmol), cyclohexylmethyl bromide (3.51 g, 19.8 mmol) and potassium carbonate (2.81 g, 20.33 mmol) was stirred under Ar at +85° C. for 3 days and cooled to room temperature. Reaction mixture was diluted with water and extracted with hexanes three times. Combined organic layers were dried over anhydrous MgSO4 and concentrated under reduced pressure. Purification by flash chromatography (2%-15% EtOAc—hexanes gradient) gave cyclohexylmethyl 5-chlorothiophene-2-carboxylate as a colorless oil. Yield (4.76 g, 97%); 1H NMR (400 MHz, CDCl3) δ 7.56-7.60 (m, 1H), 6.90-6.94 (m, 1H), 4.08 (d, J=6.10 Hz, 2H), 1.64-1.82 (m, 6H), 1.10-1.34 (m, 3H), 0.97-1.10 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447078B2
Source datasetuspto-grants-2016_09
ORD IDord-30c4ccd6c9304edebef711969c425c30
Source noteuspto-grants-2016_09