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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243818Generated: October 31, 2026

Hydrochloric Acid → 7-(Benzyloxy)-4-methyl-1,2-dihydronaphthalene

https://huagongshe.com/reaction/243818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
Reactant6-(benzyloxy)-3,4-dihydronaphthalen-1(2H)-oneHCID 10682241—
SolventHCID 178418573HCID 178418573—
Product7-(Benzyloxy)-4-methyl-1,2-dihydronaphthaleneHCID 23121671—

Reaction Steps

To a solution of the obtained 6-(benzyloxy)-3,4-dihydronaphtalen-1(2H)-one (34.5 g) in tetrahydrofuran (300 mL), methyl magnesium bromide (3M diethyl ether solution, 55 mL) was added at 0° C., followed by stirring at room temperature for 1 hour. The reaction mixture was cooled to 0° C. and poured into ice-saturated aqueous ammonium chloride solution. After adding 2N hydrochloric acid, the mixture was stirred at room temperature for 3 hours. Then, the resultant was extracted with ethyl acetate and the organic layer was successively washed with water and brine, dried and concentrated. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to thereby give the title compound (24.8 g) having the following physical properties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653305B2
Source datasetuspto-grants-2014_02
ORD IDord-8003e202c2464e00a1cdd6a6fbb8bf3c
Source noteuspto-grants-2014_02