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HRID 355239作成日:2026年10月24日

Triethylamine → (1R,2R)-ethyl 2-((methylsulfonyloxy)methyl)cyclopropanecarboxylate

https://huagongshe.com/ja/reaction/355239

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Ethyl (1R,2R)-2-(hydroxymethyl)cyclopropanecarboxylateHCID 29920784—
溶媒TetrahydrofuranHCID 8028—
生成物(1R,2R)-ethyl 2-((methylsulfonyloxy)methyl)cyclopropanecarboxylateHCID 53825740—

反応条件

温度0 °C

反応手順

A solution of trans-ethyl 2-hydroxymethyl-1-cyclopropanecarboxylate (1.136 g, 7.88 mmol) in dry tetrahydrofuran (20 ml) was cooled to 0° C. (ice bath), treated dropwise with mesyl chloride (0.675 ml, 8.66 mmol) and then treated immediately with triethylamine (1.32 ml, 9.52 mmol). This solution was stirred at 0° C. for 1.5 h (tlc indicated no substrate left). After dilution with ether (200 ml), the solution was washed with water, saturated ammonium chloride (10 ml), brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure gave a clear oil, 1.690 g (97%) which was used as such for the next step without purification. ir (film) νmax : 1720 cm-1 (C=O); 1Hmr (CDCl3) δ: 4.13 (2H, q, J=7, CH2 --CH3, 3.05 (2H, s, CH2 --OMs), 2.0~0.6 (4H, m, cyclopropyl), 1.27 ppm (3H, t, J=7, CH3 --CH2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04378314
出典データセットuspto-grants-1983_03
ORD IDord-41c9eeaee4d84aefa6df148d6cab7119
出典メモuspto-grants-1983_03