Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028466Generated: November 2, 2026

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

https://huagongshe.com/reaction/1028466

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-indanoneHCID 520695—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-bromo-2,3-dihydro-1H-inden-1-olHCID 13486299100.9%

Reaction Steps

To a solution of 5-bromoindanone (2.2 g, 0.01 mol) in a mixture of methanol (50 mL) and tetrahydrofuran (10 mL) was added sodium borohydride (0.78 g, 0.02 mol) and the reaction mixture was stirred at room temperature overnight. The solution was concentrated and the residue was partitioned between water and ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated to give 2.15 g of crude material. 1H NMR (300 MHz, CDCl3) 6 ppm 157 (s, 1 H) 1.87-2.02 (m, 1 H) 2.40-2.59 (m, 1 H) 2.73-2.88 (m, 1 H) 2.95-3.11 (m, 1 H) 5.12-5.25 (m, 1 H) 7.29 (s, 1 H) 7.32-7.43 (m, 2 H). MS (ESI), m/z 416.0 (M+205)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735595B2
Source datasetuspto-grants-2014_05
ORD IDord-4a7a2bb46c28405bbbb74c3b69e1e581
Source noteuspto-grants-2014_05