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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633494Generated: October 25, 2026

Acetic Anhydride → 2-(Acetylamino)-1,3-benzothiazol-6-yl thiocyanate

https://huagongshe.com/reaction/633494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Amino-6-thiocyanato-1,3-benzothiazoleHCID 81600—
SolventPyridineHCID 1049—
Product2-(Acetylamino)-1,3-benzothiazol-6-yl thiocyanateHCID 815098—

Reaction Steps

5 cm3 of acetic anhydride are added dropwise to 7 cm3 of pyridine at 20° C. After 5 min, 1 g of 2-amino-6-thiocyanatobenzothiazole (commercial) is added. The yellow suspension is stirred for 4 h and then concentrated to dryness under vacuum. The residue is made into a paste in ethyl ether. The insoluble material is isolated by filtration, to give 1.1 g of 2-(acetylamino)-1,3-benzothiazol-6-ylthiocyanate in the form of a yellow solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321777B2
Source datasetuspto-grants-2016_04
ORD IDord-a2f6fd3cde9745c5a6f895980ce388d4
Source noteuspto-grants-2016_04