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HRID 1876997作成日:2026年10月26日

3-Heptanone → Ethyl 2-ethyl-5-(1-ethyl-1-hydroxypropyl)thiophene-3-carboxylate

https://huagongshe.com/reaction/1876997

反応式

関与物質

役割名称HCID仕込み量
反応物3-HeptanoneHCID 7802—
反応物Ammonium ChlorideHCID 25517—
反応物Ethyl 5-bromo-2-ethylthiophene-3-carboxylateHCID 68515411—
反応物HCID 178420663HCID 178420663—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-ethyl-5-(1-ethyl-1-hydroxypropyl)thiophene-3-carboxylateHCID 68512433—

反応手順

To a solution of ethyl 5-bromo-2-ethylthiophene-3-carboxylate (3.00 g) synthesized in Example 69 (4) in tetrahydrofuran (50 mL) was added dropwise 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (13.7 mL) at −45° C. After stirring under an argon atmosphere for 1 hr, 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (13.7 mL) was added dropwise, and the mixture was stirred for 1 hr. 3-Heptanone (6.04 mL) was added dropwise, and the mixture was stirred at −45° C. for 1 hr, and at room temperature for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:17, volume ratio) to give the title compound (3.06 g, quantitative) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08309580B2
出典データセットuspto-grants-2012_11
ORD IDord-888730f20d674d77a67762f5c23b3b4f
出典メモuspto-grants-2012_11