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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896068Generated: October 30, 2026

1-Indanone, 6-bromo- → 6-bromo-2,3-dihydro-1H-inden-1-ol

https://huagongshe.com/reaction/896068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Indanone, 6-bromo-HCID 139778—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product6-bromo-2,3-dihydro-1H-inden-1-olHCID 2754824100%

Reaction Steps

To a solution of 6-bromo-1-indanone (prepared as described by Cornelius, Lyndon A. M. and Combs, Donald W. Synth. Commun. (1994), 24(19), 2777-88) (1.4 g, 6.57 mmol) in 20 mL of methanol was added sodium borohydride (0.087 g, 2.3 mmol) over a period of five minutes at room temperature. The reaction mixture was stirred for two hours at room temperature, concentrated under pressure and partitioned between ethyl acetate (50 mL) and 1N HCl (20 mL). The ethyl acetate layer was dried over sodium sulfate and concentrated under reduced pressure to yield the title compound as a solid (1.4 g, 99%). 1H NMR (CDCl3): δ 7.45 (s, 1H), 7.3 (d, 1H), 7.0 (d, 1H), 5.2 (t, 1H), 2.9 (m, 1H), 2.7 (m, 1H), 2.4 (m, 1H), 1.9 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919335B2
Source datasetuspto-grants-2005_07
ORD IDord-e2d1d48b2e634a9784938743713600a1
Source noteuspto-grants-2005_07