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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | alpha-(Tert-butoxycarbonyl)amino(1,3-dihydrobenzo[c]thien-4-yl)acetic acid | HCID 86737162 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Amino(1,3-dihydrobenzo[c]thien-4-yl)acetic acid | HCID 23345394 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04219648 |
|---|
| Source dataset | uspto-grants-1980_08 |
|---|
| ORD ID | ord-0393858ba19e462bab5296743c545fbc |
|---|
| Source note | uspto-grants-1980_08 |
|---|