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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59779Generated: October 26, 2026

Sodium borohydride → HCID 90389980, compound

https://huagongshe.com/reaction/59779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2-Phenyl-chroman-6-yloxy)-cyclohexanoneHCID 90390155—
SolventEthanolHCID 702—
ProductHCID 90389980HCID 9038998096.3%

Reaction Steps

500 mg of 4-(2-phenyl-chroman-6-yloxy)-cyclohexanone (1.6 mmol) were dissolved at 0° C. in 2.5 ml of ethanol. 30 mg of sodium borohydride (0.78 mmol) were added in portions, and stirring at room temperature was continued for 2 h. The solvent was removed under reduced pressure and the residue separated between saturated aqueous sodium hydrogencarbonate solution and dichloromethane. The aqueous layer was extracted with dichloromethane. The combined organic layers were dried with sodium sulfate and filtered, and volatile components removed under reduced pressure. 500 mg of the title compound were obtained as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440941B2
Source datasetuspto-grants-2016_09
ORD IDord-bad77bf8f38c4ed28ed07e45a81f81f7
Source noteuspto-grants-2016_09