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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608392Generated: October 31, 2026

Sodium borohydride → HCID 14425608, compound

https://huagongshe.com/reaction/1608392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14425607HCID 14425607—
SolventEthanolHCID 702—
ProductHCID 14425608HCID 1442560878.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04870219
Source datasetuspto-grants-1989_09
ORD IDord-1a07fd4c36534ab88ae7338f2de4a6cd
Source noteuspto-grants-1989_09