Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896383Generated: October 30, 2026

Acetoxyacetyl chloride → HCID 20814102, compound

https://huagongshe.com/reaction/896383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoxyacetyl chlorideHCID 26297—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3-Diaminobenzoic acid methyl esterHCID 571825—
SolventDichloromethaneHCID 6344—
ProductHCID 20814102HCID 2081410272.1%

Reaction Steps

To a mixture of 2,3-diamino-benzoic acid methyl ester (40.8 mmol) and diisopropylethyl amine (8.5 mL, 49.0 mmol) in dichloromethane (80 mL) at −30° C. was added dropwise a solution of acetoxy acetyl chloride (4.8 mL, 44.9 mmol) in DCM (15 mL). The mixture was allowed to warm to room temperature and stirred overnight. The mixture was quenched with satd. ammonium chloride (50 mL), the layers separated and the aqueous phase extracted with DCM (60 mL). The combined organic layers were washed with brine and dried (MgSO4). The residue after concentration was dissolved in acetic acid (50 mL) and heated at 100° C. for 30 min. The solution was concentrated and purified by flash chromatography (eluent DCM-ethyl acetate 3:1, 2:1, 1:1) to give 2-acetoxymethyl-1H-benzoimidazole-4-carboxylic acid methyl ester (7.3 g, 72% yield over 2 steps) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919331B2
Source datasetuspto-grants-2005_07
ORD IDord-4438e2cc96c045688484efb569c2f4b3
Source noteuspto-grants-2005_07