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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223478Generated: October 31, 2026

Trichloroacetyl chloride → HCID 13067102, compound

https://huagongshe.com/reaction/223478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
ReactantHCID 13067095HCID 13067095—
SolventDichloromethaneHCID 6344—
ProductHCID 13067102HCID 13067102—

Reaction Steps

A mixture of 3.4 g (11 mmole) of 8-chloro-6-(2-fluorophenyl)-1-methyl-2H,4H-pyrrolo[3,4-d][2]benzazepine, 2.6 g (14 mmole) of trichloroacetyl chloride, and 100 ml of methylene chloride was stirred at room temperature for 12 hr. The resulting precipitate was collected by filtration, resuspended in methylene chloride, and basified with ammonium hydroxide. The methylene chloride solution was separated, dried over anhydrous sodium sulfate, and concentrated at reduced pressure to give a (mp 222°-225°) colorless solid. A small portion was recrystallized from a mixture of methylene chloride and ether to give colorless prisms, mp 222°-223°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04354973
Source datasetuspto-grants-1982_10
ORD IDord-46a86020850a4c5d9743f61bc5ce26c7
Source noteuspto-grants-1982_10