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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498935Generated: October 29, 2026

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

https://huagongshe.com/reaction/498935

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 8661259386%

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 numberUS07767650B2
Source datasetuspto-grants-2010_08
ORD IDord-0f236feb1bac4a3987349ec056c8ecf7
Source noteuspto-grants-2010_08