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HRID 428230作成日:2026年10月26日

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

https://huagongshe.com/reaction/428230

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Ethyl chloroformateHCID 10928—
反応物1,1,4,4-Tetramethyl-6-ethynyl-1,2,3,4-tetrahydronaphthaleneHCID 14726549—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl 3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)propiolateHCID 11000580—

反応条件

温度-10 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313163B1
出典データセットuspto-grants-2001_11
ORD IDord-3e8e7146651c4e688d91778793842f9c
出典メモuspto-grants-2001_11