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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428215Generated: October 27, 2026

Water → 3-Methoxyethoxymethoxy-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-bromonaphthalene

https://huagongshe.com/reaction/428215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
Reactant3-Bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-olHCID 10779311—
SolventDimethylformamideHCID 6228—
Product3-Methoxyethoxymethoxy-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-bromonaphthaleneHCID 56988936—

Reaction Steps

720 mg (24 mmol) of sodium hydride (80% in oil) and 50 ml of DMF are introduced into a three-necked flask under a stream of nitrogen. A solution of 5.7 g (20 mmol) of 3-bromo-5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthol dissolved in 75 ml of DMF are added dropwise and the mixture is stirred until the evolution of gas has ceased. 6.8 ml (59.3 mmol) of methoxyethoxymethyl chloride are then added at 0° C. and the mixture is stirred for four hours. The reaction medium is poured into water and extracted with ethyl ether, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. 16.6 g (91%) of the expected product are collected in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313162B1
Source datasetuspto-grants-2001_11
ORD IDord-f2d46ac2c3184a9da4c1aaa56bb6bf81
Source noteuspto-grants-2001_11