HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 54185237, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57091011 | HCID 57091011 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54185237 | HCID 54185237 | — |
Reaction Steps
To a stirred solution of 0.58 g of NaBH4 (18 mmoles) in 50 ml of ethanol cooled to 0° C. are added drop by drop within one hour 5 g (24 mmoles) of 3-methyl-5-(2,2,3-trimethyl-cyclopent-1-yl)-pent-4-en-2-one. The reaction mixture is stirred for 90 minutes at room temperature. The ethanol is removed by rotary evaporation and the reaction mass is extracted with ether and washed with water. After evaporation of the solvent the crude product is vacuum distilled, to yield 3-methyl-5-(2,2,3-trimethyl-cyclopent-1-yl)-pent-4-en-2-ol: 4.4 g (mixture of isomers)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05288701 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-353640d8ac9b458db0751cb9e3dcf7f2 |
| Source note | uspto-grants-1994_02 |