HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → 2-Chloro-6-(trimethylsilyl)benzenecarbothioic acid, S-ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | 2-Chloro-6-(trimethylsilyl)benzoyl chloride | HCID 15183557 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-6-(trimethylsilyl)benzenecarbothioic acid, S-ethyl ester | HCID 86164155 | 61% |
Reaction Steps
The compound of Example b (1.48 g, 0.006 mol), CH2Cl2 (50 mL), ethanethiol (0.44 g, 0.007 mol), and 4-(N,N-dimethylamino)pyridine (0.86 g, 0.007 mol) were allowed to stir at RT overnight. The mixture was washed with 10% HCl and three times with water, dried (MgSO4), and concentrated. The crude product was purified by RC, eluting with 1:3 ethyl acetate/hexanes. The title compound was obtained as a clear oil in 61% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05849723 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-330ba0bf4e9c4418bb983d95fb973741 |
| Source note | uspto-grants-1998_12 |