Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194585Generated: October 30, 2026

Chlorine → N'-tert-butylbenzohydrazide

https://huagongshe.com/reaction/1194585

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 numberUS04814349
Source datasetuspto-grants-1989_03
ORD IDord-82b9742e4069431e9733b8dc104bf970
Source noteuspto-grants-1989_03