HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973468Generated: November 1, 2026
Water → 2-[2-(4-Bromophenyl)-2-oxoethyl]cycloheptan-1-one
https://huagongshe.com/reaction/1973468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromophenacyl bromide | HCID 7454 | — |
| Reactant | 1-(1-Pyrrolidinyl)-1-cycloheptene | HCID 586037 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-(4-Bromophenyl)-2-oxoethyl]cycloheptan-1-one | HCID 21491522 | — |
Reaction Steps
A solution of 80 g (0.28 mole) of p-bromophenacyl bromide in dry dimethylformamide is added dropwise to a cooled solution of 40.2 g (0.28 mole) of 1-pyrrolidino-1-cycloheptene in dry dimethylformamide. After stirring at ambient temperature for 24 hours, and at 100° C. for 5 hours, water is added and the mixture is stirred for an additional 4 hours. The reaction mixture is poured into 1500 ml. of water and extracted with chloroform. The chloroform solution is washed with water, dried, and evaporated to a red oil which is stirred at 100° for 1 hour under a high vacuum. Upon cooling the oil converts to a semi-solid. The semi-solid is crystallized from an ethanol - cyclohexane mixture to give 2-(p-bromophenacyl)cycloheptanone, m.p. 124°-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03997557 |
|---|
| Source dataset | uspto-grants-1976_12 |
|---|
| ORD ID | ord-ddc7babab2644f70ae3cf849b98f8eb4 |
|---|
| Source note | uspto-grants-1976_12 |
|---|