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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292738Generated: October 31, 2026

5-Bromo-1-indanone → 5-bromo-2,3-dihydro-1H-inden-1-ol

https://huagongshe.com/reaction/1292738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product5-bromo-2,3-dihydro-1H-inden-1-olHCID 13486299—

Reaction Steps

To a suspension of 40 g (184 mmol) of 5-bromo-1-indanone in 500 mL of methanol in a water bath was added 16.2 g of sodium borohydride portionwise, keeping the reaction temperature below 40° C. The water bath was removed and the reaction mixture stirred at ambient temperature for 2 h and then quenched by the addition of 100 mL of water. The methanol was removed in vacuo, and the residue partitioned between water and ethyl acetate. The aqueous phase was extracted with two portions of ethyl acetate. The combined organic phases were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, and concentrated to give a yellow solid which was used without further purification. Mass spectrum (MS): m/z 195, 197 (M+1-H2O), 116 (M+1-H2O-HBr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238683B2
Source datasetuspto-grants-2007_07
ORD IDord-41d71330e7ae4ec7a4fc2827df44e633
Source noteuspto-grants-2007_07