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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561444Generated: October 25, 2026

5-Chloro-1-indanone → 6-chloro-1-cyclopropyl-2,3-dihydro-1H-inden-1-ol

https://huagongshe.com/reaction/561444

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1-indanoneHCID 142599—
Reactant6-Chloro-1-indanoneHCID 5100705—
ReactantHCID 178418630HCID 178418630—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product6-chloro-1-cyclopropyl-2,3-dihydro-1H-inden-1-olHCID 58392268—

Reaction Steps

45 ml (22.5 mmol) of a 0.5N solution of cyclopropylmagnesium bromide in tetrahydrofuran were added to 2.50 g (15.0 mmol) of a mixture of 5-chloro-2,3-dihydro-1H-inden-1-one and 6-chloro-2,3-dihydro-1H-inden-1-one in 56 ml of diethyl ether at RT, and the mixture was stirred at RT overnight. The reaction mixture was added to ice-water, the phases were separated, the aqueous phase was extracted with dichloromethane, and the combined organic phases were dried over magnesium sulfate, filtered and concentrated. The crude product was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate gradient) and preparative HPLC (mobile phase: acetonitrile/water gradient) to result in 152 mg (5% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-e7587d8264b74b0a9c638152ff38f705
Source noteuspto-grants-2011_11