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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376901Generated: October 29, 2026

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

https://huagongshe.com/reaction/1376901

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 numberUS05663367
Source datasetuspto-grants-1997_09
ORD IDord-82a02ef58f05402c818d1112b01635c2
Source noteuspto-grants-1997_09