HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl mercaptan → alpha-Benzylthiomethyl-beta-(p-chlorophenyl)-gamma-butyrolactone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | beta-(p-Chlorophenyl)-alpha-methylene-gamma-butyrolactone | HCID 20234200 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha-Benzylthiomethyl-beta-(p-chlorophenyl)-gamma-butyrolactone | HCID 13518985 | 81% |
Reaction Steps
To a solution of 700 mg of β-(p-chlorophenyl)-α-methylene-γ-butyrolactone in 10 ml of toluene were added 0.51 ml of benzylmercaptan and one drop of triethylamine and the resulting mixture was kept at room temperature for 6 hours. After completion of the reaction, the reaction mixture was diluted with 100 ml of ethyl ether, washed with 10% aqueous sodium hydroxide and saturated saline, dried over magnesium sulfate and the solvent was distilled off. The crude product thus obtained was purified by a column chromatography to give 900 mg (yield 81%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04613613 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-e3ebcc3beb1645798651b66d77616bf4 |
| Source note | uspto-grants-1986_09 |