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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266951Generated: November 1, 2026

Benzoyl chloride → HCID 11432126, compound

https://huagongshe.com/reaction/2266951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11486440HCID 11486440—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 11432126HCID 11432126—

Reaction Conditions

Temperature20 °C

Reaction Steps

4-[2-(2-hydroxyethoxy)-ethyl]-piperazine-carboxylic acid (2-phenylsulfanyl-phenyl)-amide (4 g, 10 mmol), triethylamine (2 ml, 15 mmol) and toluene (50 ml) were charged into a reaction flask. Benzoyl chloride (1.7 g, 12 mmol) in toluene (5 ml) was added at 0-10° C. The mixture was stirred for 16 h at 20° C. Cold water (50 ml) and 1 M NaOH (100 ml) were added. The mixture was stirred for 20 min. The water phase was separated. The organic phase was washed with saturated NaCl solution (25 ml) and evaporated in vacuo. The yield of benzoic acid 2-{2-[4-(2-phenylsulfanyl-phenylcarbamoyl)piperazin-1-yl]-ethoxy}-ethyl ester was 4.91 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858777B2
Source datasetuspto-grants-2010_12
ORD IDord-e6f811528bd64dec8243e7d9a24b1b5e
Source noteuspto-grants-2010_12