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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607571Generated: October 25, 2026

Triethylamine → rac-[(5-Chloro-1,3-benzothiazol-2-yl)thio](phenyl)acetic Acid

https://huagongshe.com/reaction/1607571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromo(phenyl)acetic acidHCID 97919—
ReactantHCID 178527796HCID 178527796—
SolventDichloromethaneHCID 6344—
Productrac-[(5-Chloro-1,3-benzothiazol-2-yl)thio](phenyl)acetic AcidHCID 1292839870%

Reaction Steps

To a solution of 5-chloro-2-mercaptobenzothiazole (38 g, 0.188 mol) in methylene chloride (750 mL) was added α-bromophenylacetic acid (38 g, 0.177 L mol) and triethylamine (38.5 g, 53 mL, 0.38 mol). The mixture was heated to reflux overnight. The clear solution was evaporated in vacuo and the residue was taken up in ethyl acetate, washed with dilute hydrochloric acid solution, then with water and finally dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo to a small volume and treated with n-hexane whereby the product crystallized out. Filtration yielded the product as a beige crystalline compound (41 g, 70%), m.p. 184°-185° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866082
Source datasetuspto-grants-1989_09
ORD IDord-d0a985991e584ee596db388be46e5347
Source noteuspto-grants-1989_09