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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345752Generated: October 29, 2026

Chloride → HCID 11086987, compound

https://huagongshe.com/reaction/345752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactantn-(4-nitrobenzyl)benzamideHCID 282107—
SolventThionyl ChlorideHCID 24386—
ProductHCID 11086987HCID 1108698785%

Reaction Steps

A solution of 3.7 mmol of N-(p-nitrobenzyl)-benzamide in thionyl chloride was refluxed under an inert atmosphere for 30 minutes and after cooling, the excess thionyl chloride was removed under vacuum to leave a solid residue. The residue was crystallized from dry cyclohexane under dry nitrogen (Note: the subsequent filtration had to be done under dry nitrogen also to obtain an 85% yield of the purified imidoyl--chloride melting at 71° to 73° C. (Lit. m.pt. 73--4 Huisgen et al--Loc. cit) which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059596
Source datasetuspto-grants-1991_10
ORD IDord-09e432bad7e34f9a93b89b58e18035dc
Source noteuspto-grants-1991_10