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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856491Generated: October 26, 2026

m-Chloroperbenzoic acid → Amino(1,3-dihydrobenzo[c]thien-4-yl)acetic acid

https://huagongshe.com/reaction/1856491

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactantalpha-(Tert-butoxycarbonyl)amino(1,3-dihydrobenzo[c]thien-4-yl)acetic acidHCID 86737162—
SolventChloroformHCID 6212—
ProductAmino(1,3-dihydrobenzo[c]thien-4-yl)acetic acidHCID 23345394—

Reaction Conditions

Temperature0 °C

Reaction Steps

α-(tert-Butoxycarbonyl)amino(1,3-dihydrobenzo[c]thien-4-yl)acetic acid (0.05 m) is added to chloroform and the mixture cooled to about 0° C. Over a period of about 2.5 hours, 0.12 moles of m-chloroperbenzoic acid dissolved in chloroform is added to the mixture maintained at 0° C. When the addition of the m-chloroperbenzoic acid is complete, the temperature of the mixture is raised to about 20° to 25° C. from about 0° C. and stirred for about 18 hours, chilled to 0° C. to precipitate the m-chlorobenzoic acid which is filtered from the solution. Removal of a portion of the chloroform results in the precipitation of Amino(1,3-dihydrobenzo[c]thien-4-yl)acetic acid, 2-oxide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04219648
Source datasetuspto-grants-1980_08
ORD IDord-0393858ba19e462bab5296743c545fbc
Source noteuspto-grants-1980_08