HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 2-Phenylethanethioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzylthiocarbonyl chloride | HCID 19906501 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenylethanethioamide | HCID 731368 | — |
Reaction Steps
To a mixture of secondary amine I and TEA in anhydrous dichloromethane, are added dropwise a solution of phenylthioacetyl chloride (prepared from phenylthioacetic acid and thionyl chloride) in anhydrous dichloromethane at 0° C. The reaction mixture is warmed to room temperature, stirred for 2 hours, then sat'd NH4Cl solution and dichloromethane are added. The organic layer is washed with brine, dried over Na2SO4, and concentrated to afford α-phenylthioacetamide II, which is used for the next reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06689890B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-4e0c4256e4054aa6bcbfe1efa6f660b3 |
| Source note | uspto-grants-2004_02 |