HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → HCID 69780574, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 54261911 | HCID 54261911 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69780574 | HCID 69780574 | — |
Reaction Steps
To a stirred solution of 16-3 (200 mg, 0.4278 mmol) and ethanethiol (0.5 ml) and CH2Cl2 (3 ml) was added AlCl3 (570 mg, 4.28 mmol). After 1.0 hour, the reaction was quenched with sat. NaHCO3. Ethyl acetate was added, and the reaction mixture was then purged with argon for 1.0 hour. The organic layer was separated, washed with brine, dried (MgSO4) and then concentrated to give the phenol 16-4 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06017926 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-bb44ec51a5574ddd8a0a376ce8b1e924 |
| Source note | uspto-grants-2000_01 |