HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone Cyanohydrin → 2-(6-Hydroxyhexyl)-3-oxocyclopentane-1-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(6-Hydroxyhexyl)-2-cyclopenten-1-one | HCID 21561487 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(6-Hydroxyhexyl)-3-oxocyclopentane-1-carbonitrile | HCID 21561503 | 73% |
Reaction Steps
A mixture of 2-(6-hydroxyhexyl)-2-cyclopenten-1-one (10.5 g., 0.058 mole), acetone cyanohydrin (5.6 g., 0.065 mole), 6% aqueous sodium carbonate (5.2 ml.) and methanol (35 ml.) was stirred and heated under reflux for 4 hours. Methanol was removed in vacuo, water (70 ml.) was added and the mixture was extracted with diethyl ether and dried over magnesium sulphate. The solvent was removed by evaporation and the residue was distilled under reduced pressure to give 2-(6-hydroxyhexyl)-3-oxocyclopentanecarbonitrile (8.8 g., 73%), b.p. 135°-178°C./0.15 mm.Hg, nD25 1.4812.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03935261 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-0e813889be024d96b63531a18beb2ad3 |
| Source note | uspto-grants-1976_01 |