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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656355Generated: October 30, 2026

1-Indanone → 1-Methyl-2,3-dihydro-1H-inden-1-OL

https://huagongshe.com/reaction/1656355

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IndanoneHCID 6735—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product1-Methyl-2,3-dihydro-1H-inden-1-OLHCID 58375188%

Reaction Steps

A solution of 25.05 g (0.190 mol) of 1-indanone in 250 ml of anhydrous ether was added over 45 min to a solution of 81.0 ml (0.243 mol) of 3.0M methyl magnesium bromide in ether under N2 whilst stirring magnetically. After completion of the addition, the reaction was heated to reflux for 40 min, allowed to cool, then quenched with 30 ml of saturated ammonium chloride solution. The ether layer was decanted from a white solid, washed with water (2×100 ml), then with saturated sodium chloride solution (100 ml), dried (K2CO3) and evaporated in vacuo to leave 24.64 g (88%) of the title product as an orange oil. NMR δ(CDCl3) 1.57 (3H, s), 2.16-2.24 (2H, m), 2.77-2.89 (1H, m), 2.97-3.09 (1H, m) 7.23-7.38 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254561
Source datasetuspto-grants-1993_10
ORD IDord-3c374c888ae24c00b760eca5ef3095dc
Source noteuspto-grants-1993_10