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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107225Generated: October 31, 2026

Chloroacetyl chloride → HCID 10594703, compound

https://huagongshe.com/reaction/1107225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantCarbamic acid, [(1S)-1-[[(2,3-dimethylphenyl)amino]methyl]pentyl]-, 1,1-dimethylethyl esterHCID 10615682—
ReactantHCID 178418361HCID 178418361—
SolventEthyl AcetateHCID 8857—
ProductHCID 10594703HCID 10594703—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of the product from Step C 98.50 g, 26.5 mmol) in ethyl acetate (250 mL) was vigorously stirred at 0° C. with saturated sodium bicarbonate (150 mL). Chloroacetyl chloride (2.33 mL, 29.1 mmol) was added, and the reaction stirred at ) 0° C. for 1 h. The layers were separated, and the ethyl acetate phase was washed with saturated brine, and dried over magnesium sulfate. The crude product was dissolved in DMF (300 mL) and cooled to 0° C. under nitrogen. Sodium hydride (1.79 g, 60% dispersion in oil, 44.9 mmol) was added portionwise to maintain moderate hydrogen evolution. After 30 min, an additional amount of sodium hydride was added (0.8 g). The reaction was stirred another 30 min, then quenched with saturated ammonium chloride. The DMF was distilled in vacuo, and the residue partitioned between ethyl acetate and water. The organic phase was washed with water, saturated brine, and dried over magnesium sulfate. The crude product was chromatographed on silica gel with 20-30% ethyl acetate in hexane to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060038
Source datasetuspto-grants-2000_05
ORD IDord-187dc7d673434e71ad597eb4bf7af694
Source noteuspto-grants-2000_05