HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → S-(4-Fluorobenzyl) 3-benzylthiopropionothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | p-Fluorotoluene-alpha-thiol | HCID 85171 | — |
| Reactant | HCID 178526178 | HCID 178526178 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S-(4-Fluorobenzyl) 3-benzylthiopropionothioate | HCID 57185058 | — |
Reaction Steps
6.18 g (30 mmoles) of dicyclohexylcarbodiimide in 20 ml of methylene chloride were added to a solution, which had been cooled to 0° C., of 5.9 g (30 mmoles) of 3-benzylthiopropionic acid and 4.26 g (30 mmoles) of 4-fluorobenzylmercaptan in 25 ml of methylene chloride, and the mixture was kept overnight at room temperature. After filtering off the dicyclohexylurea and stripping off the solvent, the crude product was purified, first by chromatography, on silica gel, from 1:2 methylene chloride/petroleum ether and then by distillation in a bulb tube.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04370342 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-c5955d99f3314cb785f20a81376bf8fe |
| Source note | uspto-grants-1983_01 |