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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296308Generated: November 1, 2026

Trichloroacetyl chloride → HCID 13067102, compound

https://huagongshe.com/reaction/2296308

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 numberUS04428879
Source datasetuspto-grants-1984_01
ORD IDord-de8ff126315d46ba8b0eab791aab80f2
Source noteuspto-grants-1984_01