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HRID 256620作成日:2026年10月27日

Acetaldehyde → Methyl 2-cyclohexyl-3-hydroxypropanoate

https://huagongshe.com/reaction/256620

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物DiisopropylamineHCID 7912—
反応物Cyclohexaneacetic acid, methyl esterHCID 139743—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Methyl 2-cyclohexyl-3-hydroxypropanoateHCID 19785625—

反応手順

To a stirred solution of diisopropylamine (0.85 ml, 6.10 mmol) in 30 ml tetrahydrofuran at -78° under argon was added n-butyllithium (2.5 ml of a 2.5M solution in hexane). After 0.5 hour, methyl cyclohexylacetate (1 ml, 6.10 mmol) was added dropwise in 10 ml tetrahydrofuran. The solution was stirred for 45 minutes, after which was added acetaldehyde (1 ml) in 10 ml tetrahydrofuran. This solution was stirred for two hours at -78°, warmed to room temperature and stirred an additional 12 hours, quenched with water and acidified with 10% hydrochloric acid. The mixture was extracted twice with ethyl ether, and the combined organic portions were then washed once with 10% hydrochloric acid, twice with water, once with saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to give the alcohol as an orange oil (b.p. 85°-92°, 0.5 mm).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05258400
出典データセットuspto-grants-1993_11
ORD IDord-8c435af331554cb1a715c2d7473bf652
出典メモuspto-grants-1993_11