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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296041Generated: October 30, 2026

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

https://huagongshe.com/reaction/1296041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1-indanoneHCID 142599—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
Product5-Chloro-2,3-dihydro-1H-inden-1-olHCID 22504804—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a precooled (5–10° C.) solution of 5-chloro-indan-1-one (2.0 g, 12 mmoles) in 33 mL of anhydrous methanol was added sodium borohydride (0.43 g, 11 mmoles). The reaction mixture was stirred at 10° C. for 2 hrs and then at room temperature for 18 hrs. The reaction mixture was evaporated to afford a yellow residue. The residue was dissolved in 200 mL of diethyl ether and then washed with water (2×100 mL), with 0.10 N hydrochloric acid (2×100 mL), and then with brine (100 mL). The organic layer was separated, dried (sodium sulfate), filtered, and the filtrate was evaporated to provide the title compound in good purity. MS m/z 167 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244763B2
Source datasetuspto-grants-2007_07
ORD IDord-6f126b94db9f44529457729dac328bc6
Source noteuspto-grants-2007_07