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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399775Generated: October 25, 2026

Methyl iodide → methyl 5-chloro-2,3-dihydro-2-mehtyl-1-oxo-1H-indene-2-carboxylate

https://huagongshe.com/reaction/2399775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDimethyl CarbonateHCID 12021—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloro-1-indanoneHCID 142599—
SolventTetrahydrofuranHCID 8028—
Productmethyl 5-chloro-2,3-dihydro-2-mehtyl-1-oxo-1H-indene-2-carboxylateHCID 19384693—

Reaction Steps

To a solution of 5-chloroindanone (10 g) and dimethyl carbonate (6.0 ml) in THF (80 ml) was added a 60% oil dispersion (5.0 g) of sodium hydride at room temperature, followed by heating at reflux for 12 hours. After cooling to room temperature, methyl iodide (5.0 ml) was added thereto, and the mixture was heated again at reflux for 12 hours. The reaction mixture was poured into ice-water and extracted with dichloromethane (300 ml×3). The extract was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to chromatography on silica gel to give methyl 5-chloro-2,3-dihydro-2-mehtyl-1-oxo-1H-indene-2-carboxylate (yield, 5.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451607
Source datasetuspto-grants-1995_09
ORD IDord-4e6f8a3052034b5c93c5d14b1b1f8695
Source noteuspto-grants-1995_09