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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24718생성일: 2026년 10월 24일

Oxalyl chloride → 2-Chloro-4-(2-formyl-1-pyrrolyl)benzoic acid methyl ester

https://huagongshe.com/ko/reaction/24718

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물2-Chloro-4-(1-pyrrolyl)benzoic acid methyl esterHCID 4763735—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물2-Chloro-4-(2-formyl-1-pyrrolyl)benzoic acid methyl esterHCID 53812324—

반응 단계

A solution of DMF (0.1 mL) in CH2Cl2 (2 mL) was added dropwise with stirring to a solution of oxalyl chloride (0.2 mL) in CH2Cl2 (16 mL) at −30° C. under N2. The mixture was stirred for 15 min and a solution of 2-chloro-4-(1-pyrrolyl)benzoic acid methyl ester (0.5 g) in DMF (4 mL) was added. The mixture was stirred at that temperature for 3 h and allowed to warm to room temperature. The mixture was stirred overnight and evaporated. The residue was partitioned between EtOAc and 0.2 M NaOAc. The EtOAc layer was separated and the aqueous solution was extracted with EtOAc. The combined EtOAc layer was washed with brine, dried (MgSO4), filtered and evaporated. The residue was purified by column chromatography (silica gel; eluent: hexane/EtOAc 3/1) to yield 2-chloro-4-(2-formyl-1-pyrrolyl)benzoic acid methyl ester (0.41 g). ESMS: 264 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855843B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-bf2c496b4c8e477298ee7b7da7604739
출처 메모uspto-grants-2005_02