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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24718Generated: October 25, 2026

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

https://huagongshe.com/reaction/24718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-Chloro-4-(1-pyrrolyl)benzoic acid methyl esterHCID 4763735—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-(2-formyl-1-pyrrolyl)benzoic acid methyl esterHCID 53812324—

Reaction Steps

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+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855843B2
Source datasetuspto-grants-2005_02
ORD IDord-bf2c496b4c8e477298ee7b7da7604739
Source noteuspto-grants-2005_02