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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334522Generated: October 26, 2026

Chloroacetyl chloride → 3,4-dichloro-N'-(2-chloroacetyl)benzohydrazide

https://huagongshe.com/reaction/334522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantChlorineHCID 24526—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4-DichlorobenzohydrazideHCID 138596—
Product3,4-dichloro-N'-(2-chloroacetyl)benzohydrazideHCID 6747938650%

Reaction Steps

To a solution of compound 8 (370 mg, 0.934 mmol) in 5 ml of CH2 Cl2 was added DIPEA (180 mg, 1.4 mmol) at 0° C. and stirred for 10 minutes. Then chloroacetyl chloride (116 mg, 1.02 mmol) was added slowly at the same temperature and the mixture was warmed to ambient temperature and stirred overnight. Solvent was removed to give the crude compound which was used in the next step without any further purification. The crude compound was heated to reflux in toluene (25 ml) using Dean-Stark for 12 hours. Then the toluene was distilled and the crude material purified by column chromatography using EtOAc:Hexane (45:55) as an eluent to afford compound 9 as a pale yellow gummy material (212 mg). Yield: 50%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883827B2
Source datasetuspto-grants-2014_11
ORD IDord-2d367ac8de2744dba3e0fcb46f27a7b8
Source noteuspto-grants-2014_11