HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1-(4-hydroxyphenyl)ethanone → Cyclohexanone, 2-[2-(4-hydroxyphenyl)-2-oxoethyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1-(4-hydroxyphenyl)ethanone | HCID 4964 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Pyrrolidino-1-cyclohexene | HCID 70768 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cyclohexanone, 2-[2-(4-hydroxyphenyl)-2-oxoethyl]- | HCID 12270333 | — |
Reaction Steps
43 g (0.2 mole) of (p-hydroxyphenacyl bromide) are added dropwise during 1/2 hour to a cooled (25° C) solution of 30 g (0.2 mole) of 1-pyrrolidino-1-cyclohexene in dimethylformamide. After 51/2 hours, the solution is diluted with water and extracted with chloroform. The chloroform solution is washed with water, dried over sodium sulfate and concentrated to an oil. Distillation gives a liquid which solidifies to give 2-(p-hydroxyphenacyl) cyclohexanone, m.p. 120°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03997557 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-b4dfb3d234594e2184b03bf3ea2e986a |
| Source note | uspto-grants-1976_12 |