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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194586Generated: October 31, 2026

2,5-Dichlorobenzoyl chloride → Benzoyl chloride, 3,4-dichloro-

https://huagongshe.com/reaction/1194586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichlorobenzoyl chlorideHCID 17945—
Reactant1-Naphthalenecarbonyl chlorideHCID 70146—
Reactant3,5-Dichlorobenzoyl chlorideHCID 76191—
ReactantBenzoyl chloride, 2-chloro-4-nitro-HCID 81522—
Reactant2,6-Difluorobenzoyl chlorideHCID 87438—
Reactant3-Bromo-4-methylbenzoyl chlorideHCID 2757057—
ProductBenzoyl chloride, 3,4-dichloro-HCID 76403—

Reaction Steps

Similarly, substituting 2-chloro-4-nitrobenzoyl chloride, 3-bromo-4-methylbenzoyl chloride, 2,6-difluorobenzoyl chloride, 2,5-dichlorobenzoyl chloride, 3,5-dichlorobenzoyl chloride or naphthoyl chloride, for 3,4-dichlorobenzoyl chloride, yields respectively: 2-chloro-4-nitrobenzoic acid, 2-(tert)-butylhydrazide; 3-bromo-4-methylbenzoic acid, 2-(tert)-butylhydrazide; mp 95°-97° C.; 2,5-dichlorobenzoic acid 2-(tert)-butylhydrazide and 3,5dichlorobenzoic acid, 2-(tert)-butylhydrazide, mp 163°-165° C.; 1-naphthoic acid, 2-(tert)-butylhydrazide mp 148°-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04814349
Source datasetuspto-grants-1989_03
ORD IDord-2d1632d7aaae41f482e08320e8bf065d
Source noteuspto-grants-1989_03