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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342137Generated: October 29, 2026

Chloroacetyl chloride → HCID 69597420, compound

https://huagongshe.com/reaction/342137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantCesium carbonateHCID 10796—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57295847HCID 57295847—
SolventEthyl AcetateHCID 8857—
ProductHCID 69597420HCID 69597420—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of the product from Step H (22.0 g, 63.9 mmol) in ethyl acetate (150 mL) was vigorously stirred at 0° C. with saturated sodium bicarbonate (150 mL). Chloroacetyl chloride (5.6 mL, 70.2 mmol) was added dropwise, and the reaction stirred at 0° C. for 2 h. The layers were separated, and the ethyl acetate phase was washed with 10% citric acid and saturated brine, and dried over sodium sulfate. After concentration in vacuo, the resulting crude product (27.6 g) was dissolved in DMF (300 mL) and cooled to 0° C. under argon. Cesium carbonate (63.9 g, 196 mmol) was added, and the reaction was stirred for two days, allowing it to warm to room temperature. Another portion of cesium carbonate (10 g, 30 mmol) was added, and the reaction was stirred for 16 hours. The DMF was distilled in vacuo, and the residue partitioned between ethyl acetate and water. The organic phase was washed with saturated brine, and dried over sodium sulfate. The crude product was chromatographed on silica gel with 20-25% ethyl acetate in hexane to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856326
Source datasetuspto-grants-1999_01
ORD IDord-d9c66ebd81234699a09b17f9d94b8da3
Source noteuspto-grants-1999_01