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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646983Generated: October 25, 2026

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

https://huagongshe.com/reaction/1646983

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 mixture of 8.0 g of 5-chloroindanone and 4.2 ml of dimethylcarbonate in 60 ml of THF was added 4.0 g of 60% NaH and the mixture was heated to reflux under N2 overnight. After this time the reaction was cooled to room temperature and 4.0 ml of methyl iodide was added and the mixture was reheated to reflux overnight. The reaction was then cooled and partitioned between ether and 5% aqueous NaHCO3 and the aqueous extracts were washed twice with ether. The combined aqueous extracts were dried over MgSO4 and concentrated to 11.24 g of a brown oil. Chromatogrpahy on silica gel (10% ethyl acetate/hexane) afforded 4.25 g of the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05182303
Source datasetuspto-grants-1993_01
ORD IDord-25245a473ca4448d834669a23fe38a17
Source noteuspto-grants-1993_01