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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772394Generated: November 3, 2026

1-Indanone, 4-bromo- → 4-Bromo-1-indanol

https://huagongshe.com/reaction/1772394

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Indanone, 4-bromo-HCID 98713—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product4-Bromo-1-indanolHCID 1333020896.1%

Reaction Steps

A solution of compound 2 (435 g, 2.06 mol, 1 equiv) in ethanol (5 L) was treated with sodium borohydride (101.6 g, 2.68 mol, 1.3 equiv) and stirred overnight at room temperature. The reaction was concentrated under reduced pressure and the residue partitioned between 4 L of dichloromethane and 4 L of 10% aqueous hydrochloric acid. The layers were separated and the aqueous layer was extracted with dichloromethane (3×1 L). The combined organic layers were washed with saturated brine (2 L), dried over sodium sulfate and concentrated under reduced pressure. The resulting solid was dried overnight in a vacuum oven at 30° C. to give compound 3 (422 g, 96% yield) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249239B2
Source datasetuspto-grants-2016_02
ORD IDord-98ceb5e6ec984ae5acfa99155aede2e9
Source noteuspto-grants-2016_02