HuagongsheHuagongshe Chemistry Print Report · For research reference only
beta-(p-Chlorophenyl)-alpha-methylene-gamma-butyrolactone → S-[[4-(4-chlorophenyl)-2-oxooxolan-3-yl]methyl] benzenecarbothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | beta-(p-Chlorophenyl)-alpha-methylene-gamma-butyrolactone | HCID 20234200 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | S-[[4-(4-chlorophenyl)-2-oxooxolan-3-yl]methyl] benzenecarbothioate | HCID 13715528 | 75% |
Reaction Steps
To a solution of 600 mg of β-(p-chlorophenyl)-α-methylene-γ-butyrolactone in 10 ml of toluene were added 0.44 ml of thiobenzoic acid and one drop of triethylamine and the reaction was effected at room temperature for 18 hours. The reaction mixture was diluted with 100 ml of ethyl ether, washed with water and saturated saline, dried over magnesium sulfate and the solvent was then distilled off. The crude product thus obtained was purified by a silica gel column chromatography to give 750 mg (yield 75%) 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-3b7073b3151c4a99bac17ba77a9f95d0 |
| Source note | uspto-grants-1986_09 |