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HRID 326942作成日:2026年10月27日

Triethylamine → Methyl 1-((acetylthio)methyl)cyclopropaneacetate

https://huagongshe.com/reaction/326942

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物MethanesulfonateHCID 85257—
反応物Sodium BicarbonateHCID 516892—
反応物(1-Hydroxymethylcyclopropyl)acetic acid methyl esterHCID 29941748—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物Methyl 1-((acetylthio)methyl)cyclopropaneacetateHCID 53482060—

反応条件

温度-10 °C

反応手順

To a solution of the alcohol of Step 4 (28.2 g, 0.20 mol) and triethylamine (82 mL, 0.59 mol) in dichloromethane (1 L) cooled to -40° C. was added methanesulfonyl chloride (43.5 mL, 0.3 mol). The reaction mixture was warmed to -10° C. for 20 min and then an aqueous solution of NaHCO3 was added. The product was extracted with CH2Cl2, washed with brine and dried over Na2SO4. A portion of this mesylate (0.053 mol) was then dissolved in DMF (180 mL) and cooled to 0° C. Freshly prepared cesium thiol acetate (J. Org. Chem., 51, 3664, (1986)) (22 g, 0.11 mol) was added and the mixture was stirred overnight at r.t. The reaction mixture was poured into an aqueous solution of NaHCO3 and extracted with Et2O. The organic phases were washed with brine and dried over Na2SO4. The residual oil was then purified by flash chromatography with 10:1 hexane:EtOAc to yield 7.5 g, 70%, of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05270324
出典データセットuspto-grants-1993_12
ORD IDord-c7a5d75aec7f44b6a51c59dab759c847
出典メモuspto-grants-1993_12