HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylethanol → S-(1-phenylethyl) ethanethioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylethanol | HCID 7409 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S-(1-phenylethyl) ethanethioate | HCID 11126866 | 98.7% |
Reaction Steps
In a synthesis carried our according to Gauthier, Bourdon, Young, Tetrahedron Lett., 27(1), 15 (1986), at room temperature, 16.3 g of zinc iodide, 100 mL of dichloromethane and 12.5 g of 1-Phenyl-1-ethylalcohol are added to a 250 ml round-bottom flask. To this suspension 9.52 g of thioacetic acid is added. The mixture is stirred for 16 hours at room temperature. The reaction mixture is extracted with dichloromethane. The organic layer is washed with brine, dried over magnesium sulphate, filtered and concentrated to give 18.2 g of a yellow liquid which is purified by chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585535B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-e5ee46882bdc4ee1b564f5e54c6424a4 |
| Source note | uspto-grants-2009_09 |