HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → alpha-Phenyl-alpha-[(4,5,6,7-tetrahydrobenzothiazol-2-yl)thio]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Bromo(phenyl)acetic acid | HCID 97919 | — |
| Reactant | 4,5,6,7-Tetrahydro-1,3-benzothiazole-2-thiol | HCID 178527817 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | alpha-Phenyl-alpha-[(4,5,6,7-tetrahydrobenzothiazol-2-yl)thio]acetic acid | HCID 13560800 | 77% |
Reaction Steps
A methylene chloride solution of 5.13 g (0.03 m) 2-mercapto-4,5,6,7-tetrahydrobenzothiazole, 6.45 g. (0.03 m) α-bromophenylacetic acid and 6.0 g (0.06 m) triethylamine is heated to gentle reflux overnight. The solution is extracted twice with a dilute hydrochloric acid solution, once with water and is then dried over anhydrous MgSO4. The residual solid after solvent removal is recrystallized from acetonitrile. 7.0 g (77% yield) of title compound, melting at 118°-20° C., is obtained
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04567267 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-92a1df7ce37a479d824f7170e6c77799 |
| Source note | uspto-grants-1986_01 |