HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-(3-bromophenyl)-2-methylpropan-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | N-[2-(3-Bromophenyl)-1,1-dimethylethyl]-2-chloroacetamide | HCID 58907445 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-bromophenyl)-2-methylpropan-2-amine | HCID 23087717 | 96% |
Reaction Steps
A solution of N-[2-(3-bromophenyl)-1,1-dimethylethyl]-2-chloroacetamide (Preparation 17) (32.0 g, 105 mmol), thiourea (9.60 g, 126 mmol) and acetic acid (50 mL) in ethanol (250 mL) was heated to reflux overnight. The reaction mixture was cooled to room temperature and filtered, the filtrate was concentrated in vacuo and basified using aqueous sodium hydroxide solution (1M, 450 mL). The product was extracted with dichloromethane (2×500 mL) and the combined organics washed with brine (50 mL), dried (sodium sulfate) and the solvent removed in vacuo to afford the title compound as a black oil (23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538141B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-7e88779c2a8341b19d41e88cb7330e7a |
| Source note | uspto-grants-2009_05 |