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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843412Generated: October 30, 2026

Triethylamine → 3-(Chloromethyl)-1-methoxynaphthalene

https://huagongshe.com/reaction/843412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(4-Methoxynaphthalen-2-yl)methanolHCID 18755436—
SolventDichloromethaneHCID 6344—
Product3-(Chloromethyl)-1-methoxynaphthaleneHCID 18755443—

Reaction Conditions

Temperature-5 °C

Reaction Steps

15.0 g (79.7 mmol) of (4-methoxy-naphthalen-2-yl)-methanol [Chem. Pharm. Bull. 19(6), 1245-1256 (1971)] were dissolved in 100 ml of dichloromethane, the solution treated with 20 ml of triethylamine, cooled to −5° C. and treated slowly with 9.3 ml (119.5 mmol) methanesulfonyl chloride. Then, the reaction mixture was stirred at room temperature for 23 hours, concentrated in a water-jet vacuum, redissolved in 80 ml of tetrahydrofuran, treated with 11.25 g of sodium hydrogen carbonate and stirred for another 2 hours. The suspension was then diluted with 500 ml of water and extracted three times with 300 ml of ethyl acetate, the organic phases were washed once with distilled water, then dried over magnesium sulphate, filtered and concentrated in a water-jet vacuum. The thus-obtained crude product was chromatographed on silica gel with pentane/dichloromethane (4/1). There were thus obtained 11.9 g (57.5 mmol), 72.5% 3-chloromethyl-1-methoxy-naphthalene as a colorless solid; MS: 206 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376672B1
Source datasetuspto-grants-2002_04
ORD IDord-e97b10cb51104a8baae1b0e1d42d3f93
Source noteuspto-grants-2002_04