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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929955Generated: November 4, 2026

Sodium hydride → 5,5,8,8-Tetramethyl-4-(2-ethoxyethoxy)-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde

https://huagongshe.com/reaction/1929955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromoethyl ethyl etherHCID 61141—
Reactant4-Hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthalenecarbaldehydeHCID 86599543—
SolventDimethylformamideHCID 6228—
Product5,5,8,8-Tetramethyl-4-(2-ethoxyethoxy)-5,6,7,8-tetrahydronaphthalene-2-carbaldehydeHCID 86612593—

Reaction Steps

36 g (156 mmol) of 4-hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carbaldehyde are dissolved in 400 mL of anhydrous DMF. 6.5 g (163 mmol) of 60% sodium hydride are added portionwise and the reaction medium is stirred for 1 hour. 25 g (163 mmol) of 2-ethoxyethyl bromide are added portionwise 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=40.7 g; yield =86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188106B2
Source datasetuspto-grants-2012_05
ORD IDord-5236e3d7f764472f9d364794da529f75
Source noteuspto-grants-2012_05