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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616690Generated: October 31, 2026

2-Chloroethyl methyl ether → 5,5,8,8-Tetramethyl-4-(2-methoxyethoxy)-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde

https://huagongshe.com/reaction/1616690

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl methyl etherHCID 12316—
ReactantSodium hydrideHCID 24758—
Reactant4-Hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenecarbaldehydeHCID 86599543—
SolventDimethylformamideHCID 6228—
Product5,5,8,8-Tetramethyl-4-(2-methoxyethoxy)-5,6,7,8-tetrahydronaphthalene-2-carbaldehydeHCID 8661259295%

Reaction Steps

34 g (148 mmol) of 4-hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde are dissolved in 400 mL of anhydrous DMF. 7.2 g (178 mmol) of 60% sodium hydride are then added portionwise, and the reaction medium is stirred for 1 hour. 16.5 mL (178 mmol) of 2-methoxyethyl chloride are added dropwise, and the medium is stirred at room temperature for 2 hours and then hydrolysed and extracted with ethyl ether. The organic phase is washed with 1N sodium hydroxide solution and then three times with water. The residue obtained is purified by chromatography (eluent: heptane). A yellow oil is obtained (m=42.7 g; yield=95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765805B2
Source datasetuspto-grants-2014_07
ORD IDord-eea0e7475ec24e3b8b0ca7ab14fb2ea6
Source noteuspto-grants-2014_07