HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 13335393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 4-Hydroxy-4-methyl-5-(prop-2-en-1-yl)cyclopent-2-en-1-one | HCID 12879872 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13335393 | HCID 13335393 | 94.1% |
Reaction Steps
Into a flask equipped with a stirrer and a thermometer, dl-2-allyl-3-hydroxy-3-methyl-4-cyclopentenone (30.4 g), pyridine (30 g) and dichloromethane (300 g) were charged, and acetyl chloride (30 g) was dropwise added thereto at a temperature from 10° to 20° C. in 2 hours. Then, stirring was continued at a room temperature for 24 hours. To the reaction mixture kept below 10° C., water (100 ml) was added to decompose excess of acetyl chloride. From the resultant mixture, the organic layer was separated and washed with 1% hydrochloric acid, 1% sodium bicarbonate solution and water in order. Removal of the solvent by distillation gave dl-3-acetoxy-2-allyl-3-methyl-4-cyclopentenone (36.5 g). Yield, 94%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04511655 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-1dd76370304e4e2db59841bb2d7d4c34 |
| Source note | uspto-grants-1985_04 |