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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63315생성일: 2026년 10월 25일

Cyclohexanemethanol → Cyclohexylmethyl 4-bromothiophene-2-carboxylate

https://huagongshe.com/reaction/63315

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanemethanolHCID 7507—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물4-Bromo-2-thiophenecarboxylic AcidHCID 610409—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Cyclohexylmethyl 4-bromothiophene-2-carboxylateHCID 86694606—

반응 단계

A solution of oxalyl chloride (1.4 mL, 16.1 mmol) in anhydrous CH2Cl2 (10 mL) was added dropwise to a solution of 4-bromothiophene-2-carboxylic acid (3.08 g, 14.9 mmol) and DMF (0.2 mL) in anhydrous CH2Cl2 (40 mL) over 30 mins. The reaction mixture was stirred at room temperature for 35 min then concentrated under reduced pressure. CH2Cl2 (30 mL) was added to the residue followed by cyclohexylmethanol (1.9 mL, 15.44 mmol) and Et3N (2.5 mL, 17.94 mmol). The reaction mixture was stirred at room temperature overnight and partitioned between EtOAc and aqueous 25% NH4Cl. Organic layer was washed with brine, concentrated under reduced pressure and purified by flash chromatography (2%-20% EtOAc—hexanes gradient) to give cyclohexylmethyl 4-bromothiophene-2-carboxylate as a colorless oil which was directly used in the next step. Yield (3.61 g, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447078B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-d94794a3cec146f9bc1c9a5269329a91
출처 메모uspto-grants-2016_09