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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254920Generated: November 2, 2026

Chlorine → N'-tert-butylbenzohydrazide

https://huagongshe.com/reaction/2254920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorineHCID 24526—
ReactantHCID 2797474HCID 2797474—
ReactantHCID 15617772HCID 15617772—
ReactantHCID 15617773HCID 15617773—
ReactantHCID 178418361HCID 178418361—
ProductN'-tert-butylbenzohydrazideHCID 299436—

Reaction Steps

The above reactions are illustrated below: ##STR15## wherein Q is halogen, preferably chlorine; R is tert-butyl or tert-amyl. Other compounds that can be prepared by the above procedure using the appropriately substituted benzoyl halide include: m-chlorobenzoic acid, 2-tert-butylhydrazide, mp 120°-123° C.; p-cyanobenzoic acid, 2-tert-butylhydrazide, mp 135°-136° C.; anthranilic acid, 2-tert-butylhydrazide, mp 165°-167° C.; tert-butyl or isopropyl; and X is hydrogen, halogen, C1 -C3 alkyl, methoxy, methylamino, NH2, nitro or CF3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05237099
Source datasetuspto-grants-1993_08
ORD IDord-9be9a6f759644e5e97ac27d7e5a81dbb
Source noteuspto-grants-1993_08