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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839677Generated: October 29, 2026

Benzene → 2-(4-Methoxyphenyl)-2-methyl-5-benzyloxy-6,7-dichloro-1-indanone

https://huagongshe.com/reaction/839677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantWaterHCID 962—
Reactant2-Methyl-5-benzyloxy-6,7-dichloro-1-indanoneHCID 12423614—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product2-(4-Methoxyphenyl)-2-methyl-5-benzyloxy-6,7-dichloro-1-indanoneHCID 12423615—

Reaction Conditions

Temperature25 °C

Reaction Steps

Potassium tert-butoxide (8.42 g., 0.075 mole) dissolved in tert-butanol (450 ml.) is added to a refluxing solution of 2-methyl-5-benzyloxy-6,7-dichloro-1-indanone (16.1 g., 0.05 mole) in tert-butanol (150 ml.)-benzene (600 ml.), refluxing is continued for 2.5 hrs., then 4,4'-dimethoxydiphenyliodonium chloride (37.66 g., 0.10 mole) is added and refluxing is continued for 3 hrs. The reaction mixture is cooled to 25° C., 500 ml. water added, and the mixture concentrated in vacuo to give a brown oil which on ether extraction, drying over anhydrous magnesium sulfate, removal of the ether and chromatographing of the residue on silica gel with chloroform gives 3.44 g. of 2-(4-methoxyphenyl)-2-methyl-5-benzyloxy-6,7-dichloro-1-indanone which melts at 115°-119° C. and is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04096267
Source datasetuspto-grants-1978_06
ORD IDord-e1b2e1d3c92745e9b6f34085af2a586d
Source noteuspto-grants-1978_06