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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359618Generated: October 30, 2026

Dimethylformamide → 1,2,3,4-tetrahydro-1,1,4,4,7-pentamethyl-6-[(E)-alpha-methylstyryl]naphthalene

https://huagongshe.com/reaction/359618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiethyl benzylphosphonateHCID 14122—
ReactantSodium hydrideHCID 24758—
ReactantEthanone, 1-(5,6,7,8-tetrahydro-3,5,5,8,8-pentamethyl-2-naphthalenyl)-HCID 87186—
Product1,2,3,4-tetrahydro-1,1,4,4,7-pentamethyl-6-[(E)-alpha-methylstyryl]naphthaleneHCID 14425605—

Reaction Steps

A solution of diethyl benzylphosphonate in 30 ml of dimethylformamide is added at room temperature to a suspension of 3.7 g of NaH (50% in mineral oil) in 50 ml of dimethylformamide. After stirring at room temperature for 15 minutes a solution of 12.6 g of 7-acetyl-1,1,4,4,6-pentamethyltetralin in 60 ml of dimethylformamide is added dropwise thereto in the course of 2 hours. The reaction mixture is stirred at room temperature overnight and subsequently heated to 60° for a further 1 hour. After cooling the mixture is poured on to ice, extracted with ether, dried and evaporated. After chromatography of the crude product (silica gel, elution agent hexane) and crystallization from hexane there are obtained 3.9 g of 1,2,3,4-tetrahydro-1,1,4,4,7-pentamethyl-6-[(E)-α-methylstyryl]naphthalene in colourless crystals, melting point 75°-77°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001276
Source datasetuspto-grants-1991_03
ORD IDord-736ffe3d4bff4e82b16b04bfe8cc5ad5
Source noteuspto-grants-1991_03