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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047466Generated: October 31, 2026

Water → 2-(1-methoxy-2-methyl-2,3-dihydro-1H-inden-4-yl)ethanol

https://huagongshe.com/reaction/1047466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthylene OxideHCID 6354—
Reactant4-Bromo-2-methyl-1-(methyloxy)-2,3-dihydro-1H-indeneHCID 6422814—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(1-methoxy-2-methyl-2,3-dihydro-1H-inden-4-yl)ethanolHCID 58418769—

Reaction Conditions

Temperature-110 °C

Reaction Steps

To a solution of 20.0 g (82.9 mmol) of 4-bromo-2-methyl-methoxyindane in 200 ml of THF 33.2 ml of 2.5 M (83.0 mmol) n-BuLi in hexanes was added for 20 min at −80° C. This mixture was stirred for 40 min at this temperature, cooled to −110° C., and 4.38 g (99.4 mmol) of ethylene oxide was added by one portion at vigorous stirring. The resulting mixture was stirred for 12 h at room temperature, and then 10 ml of water was added. The organic layer was separated and evaporated to dryness. To the residue 200 ml of water was added, and the crude product was extracted with 3×100 ml of dichloromethane. The combined organic extract was dried over Na2SO4 and evaporated to dryness. The product was isolated by flash chromatography using short column with Silica Gel 60 (40-63 um, d 110 mm, 190 mm; eluent: hexanes/ether=20/1). Yield 12.7 g (74%) of a ca. 1 to 1.2 mixture of two diastereomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569532B2
Source datasetuspto-grants-2013_10
ORD IDord-4752fe46a52443be9a78d3a625278808
Source noteuspto-grants-2013_10