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HRID 1451599作成日:2026年10月27日

tert-Butanol → Diethyl 2-acetamido-2-(4-tetradecenyl)malonate

https://huagongshe.com/reaction/1451599

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物Decyltriphenylphosphonium bromideHCID 3084561—
反応物Diethyl 2-acetamido-2-(4-formylbutyl)malonateHCID 21849556—
反応物HCID 178418244HCID 178418244—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Diethyl 2-acetamido-2-(4-tetradecenyl)malonateHCID 54058754—

反応条件

温度-78 °C

反応手順

Decyltriphenylphosphonium bromide (10.85 g) was dissolved in 100 ml of dry tetrahydrofuran. Under an argon atmosphere, 13 ml of a 1.6 M n-butyl lithium/hexane solution was dropwise added thereto and the mixture was stirred for 15 minutes. The mixture was cooled to -78° C. and a solution of diethyl 2-acetamido-2-(4-formylbutyl)malonate (4.17 g)/dry tetrahydrofuran (50 ml) was dropwise added thereto and the mixture was stirred at 78° C. for 40 minutes under an argon atmosphere. Under the same conditions, a solution of t-butanol (3.3 ml)/tetrahydrofuran (15 ml) was dropwise added thereto and the mixture was stirred at room temperature under an argon atmosphere for 1.5 hours. The reaction mixture was diluted with ether and washed with water. The organic layer was dried and concentrated. The concentrate was purified by silica gel column chromatography using hexane-acetic acid (5:1→5:2) as an eluent to give 2.1 g of colorless, oily diethyl 2-acetamido-2-(4-tetradecenyl)malonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05604229
出典データセットuspto-grants-1997_02
ORD IDord-4d30d5030860413990addb2380ec7f6a
出典メモuspto-grants-1997_02