HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → (3,4-Dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | N-(3,4-Dichlorophenyl)thiourea | HCID 710776 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3,4-Dichloro-phenyl)-(4-phenyl-thiazol-2-yl)-amine | HCID 86228547 | 85% |
Reaction Steps
To (3,4-Dichloro-phenyl)-thiourea (2 g, 9.04 mmol) in ethanol (35 mL) was added 2-Bromo-1-phenyl-ethanone and the solution was refluxed overnight. The reaction mixture was allowed to cool to room temperature and the resulting solid was filtered and washed with cold ethyl acetate to yield 2.45 g (85%) of an off-white solid. 1H NMR (300 MHz, DMSO-d6) δ 8.16 (d, J=1.8 Hz, 1H), 7.87 (d, J=7.5 Hz, 2 H), 7.61-7.29 (m, 6H); LCMS m/z 319 [M−1]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07381736B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-8a202ee4d2fb468b8ed0a91ab4595007 |
| Source note | uspto-grants-2008_06 |