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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271269Generated: November 1, 2026

Water → 5-(Benzyloxy)-2-(chloromethyl)-3,4-dihydronaphthalene

https://huagongshe.com/reaction/1271269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant5-(Benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthaleneHCID 22932021—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product5-(Benzyloxy)-2-(chloromethyl)-3,4-dihydronaphthaleneHCID 2293202954.5%

Reaction Steps

Under an argon atmosphere, to a solution of 1.82 g of 5-(benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthalene and 0.55 g of 4-(dimethylamino)pyridine in 30 ml of dichloromethane, 1.43 g of p-toluenesulfonyl chloride was added. After 1.2 ml of triethylamine was added dropwise, the mixture was stirred at room temperature for 1.5 hours. The reaction solution was poured into iced water and then extracted with diethyl ether. The extract was washed in turn with 5% hydrochloric acid, water and an aqueous saturated sodium hydrogen carbonate solution and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1.06 g of the desired compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205302B2
Source datasetuspto-grants-2007_04
ORD IDord-86fa57b7215a4f6eb1838bf422b7b0c7
Source noteuspto-grants-2007_04