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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008536Generated: October 30, 2026

Chloroacetyl chloride → HCID 22665701, compound

https://huagongshe.com/reaction/1008536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22665691HCID 22665691—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 22665701HCID 22665701—

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 2.43 g of 2-(benzylamino-methyl)-4-methoxy-phenol and 20 mL of toluene was cooled to 5° C. and a solution of chloroacetyl chloride (0.88 mL) in 5 mL of toluene slowly added while stirring. Stirring was continued for 2 hours at room temperature. Dry tetrahydrofuran (25 mL) was added and 3.4 g of sodium hydride (95%; dispersion in mineral oil) were added in small portions under a nitrogen atmosphere. The mixture was allowed to stir at room temperature for 24 h. Water was added and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were dried (sodium sulfate) and the solvent removed in vacuo yielding 2.0 g of 4-benzyl-7-methoxy-4,5-dihydro-benzo[f][1,4]oxazepin-3-one as an oil. EI-MS: 283 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797710B2
Source datasetuspto-grants-2004_09
ORD IDord-def80eae14b94e65beb78a0763c44277
Source noteuspto-grants-2004_09