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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291582Generated: October 31, 2026

Isoamyl Nitrite → Benzothiazolone

https://huagongshe.com/reaction/2291582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 21278869HCID 21278869—
SolventChloroformHCID 6212—
ProductBenzothiazoloneHCID 13625155.3%

Reaction Steps

To a solution of 3-[(1-piperazinyl)carbonylmethyl]-2-benzothiazolinone (3.0 g) in chloroform (50 ml) was added dropwise isoamyl nitrite (7.3 ml), for a period of 10 minutes below 20° C. The mixture was stirred for 18 hours at ambient temperature. Then, the reaction mixture was extracted with chloroform. The extract was washed with water, dried over magnesium sulfate and evaporated to give a crystalline product, which was recrystallized from a mixture of ethyl acetate and ethanol to give 3-[4-nitroso-1-piperazinyl)carbonylmethyl]-2-benzothiazolinone (2.54 g) as needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797399
Source datasetuspto-grants-1989_01
ORD IDord-f80d8b6e0dc34288bae22bdcf3a75cf6
Source noteuspto-grants-1989_01