HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 21276526, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 21276516 | HCID 21276516 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21276526 | HCID 21276526 | — |
Reaction Steps
N-methyl-2-(4-methylaminocarbonylmethoxyphenyl)-1-methylethanamine hydrochloride (2.73 g) was suspended in tetrahydrofuran (10 ml) containing triethylamine (6 ml) and a solution of α-bromoacetophenone (1.99 g) in tetrahydrofuran (10 ml) was added dropwise. After stirring overnight this solution was treated with saturated sodium carbonate solution, extracted with dichloromethane, the organic phase was dried (magnesium sulphate), filtered and evaporated to give a red oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04803293 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-d6086f0e5bab4a30ba3fd15725708941 |
| Source note | uspto-grants-1989_02 |