HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 13914899, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13030807 | HCID 13030807 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13914899 | HCID 13914899 | — |
Reaction Steps
To a stirred solution of (6,7-dichloro-2-cyclopentyl-2,3-dihydro-2-methyl-1-oxo-1H-inden-5-yl)acetamide (6.8 g., 0.02 mole) in ethanol (100 ml) is added sodium borohydride (760 mg. 0.02 mole). After one hour another portion of sodium borohydride (760 mg, 0.021 mole) is added and stirring continued for 3 hours. The reaction mixture is poured into ice water and extracted with ethyl acetate. The ethyl acetate extract is washed with water and dried over magnesium sulfate. The ethyl acetate is evaporated at reduced pressure to give (6,7-dichloro-2-cyclopentyl-2,3-dihydro-1-hydroxy-2-methyl-1H-inden-5-yl)acetamide consisting of a mixture of two diastereomer, each of which is a racemate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04680414 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-aa5e824f9d3c4bceb2cd4ef72513cad6 |
| Source note | uspto-grants-1987_07 |