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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488797Generated: November 4, 2026

Hexane → Ethyl 3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)propiolate

https://huagongshe.com/reaction/1488797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthyl chloroformateHCID 10928—
Reactant1,1,4,4-Tetramethyl-6-ethynyl-1,2,3,4-tetrahydronaphthaleneHCID 14726549—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductEthyl 3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)propiolateHCID 11000580—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a cold solution (-78° C.) of 2-ethynyl,5,5,8,8-tetramethyl-5,6, 7,8-tetrahydronaphthalene (900 mgs, 4.3 mmols) in ether (20 ml) was added n-butyllithium in hexane (5.6 mmols). The mixture was stirred for 45 mins, and ethylchloroformate (1.3 g, 12 mmols) was added via syringe. Stirring was continued for 45 mins then the mixture was warmed gradually to -10° C. and quenched by adding sodium bicarbonate (NaHCO3) solution (10 ml). Diethyl ether (100 ml) was added, the organic phase washed with water (10 ml), brine (10 ml), and dried (MgSO4). The solvent was removed in vacuo. Purification of the residue over silicagel (5% ethylacetate in hexane) gave the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05675033
Source datasetuspto-grants-1997_10
ORD IDord-a4018f8838e94a6aaa6325c73f17fe67
Source noteuspto-grants-1997_10