HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 14425608, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14425607 | HCID 14425607 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14425608 | HCID 14425608 | 78.1% |
Reaction Steps
1.4 g of 1,1,3,3-tetramethyl-5-[(E)-α-methylstyryl]2-indanone are dissolved in 100 ml of ethanol and treated at room temperature with 6 g of sodium borohydride. After stirring at room temperature for 16 hours the reaction mixture is poured on to ice and extracted repeatedly with ether. The organic phase is washed with saturated sodium chloride solution, dried and evaporated. The residue can be recrystallized from hexane and gives 1.1 g of 1,1,3,3-tetramethyl-5-[(E)-α-methylstyryl]-2-indanol in colourless crystals, melting point 63°-67°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05055622 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-f83934127e704695acd50de562760ec6 |
| Source note | uspto-grants-1991_10 |