HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 131713592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | cis-4-phenylthio-l-prolin | HCID 11379084 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 131713592 | HCID 131713592 | — |
Reaction Steps
Six hundred ml. of benzyl alcohol are cooled to 10° and, with vigorous stirring, there is added over the course of 30 minutes, 100 grams of thionyl chloride, while the temperature is maintained at 10°. To this solution there is added, at 10°, 50 grams of cis-4-(phenylthio)-L-proline and the mixture stirred for 48 hours at room temperature. To this reaction mixture there is then added 4 liters of anhydrous ether and the mixture stirred vigorously with cooling. The precipitated solid is filtered, washed with ether and dried to yield the desired 4-(S)-(phenylthio)-L-proline, phenylmethyl ester hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04462943 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-9281d18e67d945ab96d6a1ad90a307dc |
| Source note | uspto-grants-1984_07 |