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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370709Generated: October 29, 2026

Cyanogen Bromide → HCID 13324092, compound

https://huagongshe.com/reaction/370709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13324091HCID 13324091—
SolventChloroformHCID 6212—
ProductHCID 13324092HCID 13324092108.8%

Reaction Steps

To a stirred mixture of CNBr (5.9 g, 0.056 mole), K2CO3 (8.6 g) and CHCl3 (80 ml) was added dropwise 3-(1-methyl-4-piperidinyl)-1,2-benzisothiazole (11.0 g, 0.051 mole) in CHCl3 (30 ml). The mixture was stirred and refluxed for 4 hours and thereafter cooled and filtered. The filtrate was concentrated in vacuo to a solid. The solid was triturated with hexane and collected to yield 13.5 g of the desired compound. Recrystallization from MeOH--H2O (twice) yielded 4.5 g (36%) of the benzisothiazole, m.p. 118°-120°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528292
Source datasetuspto-grants-1985_07
ORD IDord-79db1c5b52ff4d72aec99cb44e7ee2a7
Source noteuspto-grants-1985_07