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HRID 19719作成日:2026年10月26日

Acetyl chloride → Methyl 2-acetyl-3-phenylbutyrate

https://huagongshe.com/reaction/19719

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物DiisopropylamineHCID 7912—
反応物Methyl 3-phenylbutanoateHCID 137945—
反応物Sodium BicarbonateHCID 516892—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-acetyl-3-phenylbutyrateHCID 12561390—

反応手順

n-Butyllithium (2.5 M hexanes 12.4 ml, 30.9 mmol) is added to N,N-diisopropylamine (4.4 ml, 31.4 mmol) in tetrahydrofuran (THF, 50 ml) at 0° C. After 10 minutes, the resultant solution is transferred via cannula to a cooled (−78° C.) solution of methyl 3-phenylbutyrate (5.0 g, 28.05 mmol) in THF (50 ml). After 40 minutes, the resultant solution is transferred via cannula to a solution of acetyl chloride (19.15 ml) in THF (50 ml). The resultant mixture is stirred at −78° C. for 1.5 hours, then warmed to 0° C. after which water is added and the mixture is then poured into saturated NaHCO3 and extracted with EtOAc. The combined organic phases are washed with brine, dried (MgSO4) and evaporated. Purification by flash chromatography (12:1 EtOAc-hexane elution) affords the title compound. δH 1.3 (d J 7 3H), 2.3 (s 3H), 3.4 (s 3H), 3.6 (m 1H), 3.8 (m 1H), 7.2-7.4 (m 5H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745462B2
出典データセットuspto-grants-2010_06
ORD IDord-f09846a5cb0b4d94b5b6987d8445cfd8
出典メモuspto-grants-2010_06