戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1893664作成日:2026年10月25日

Sodium methanethiolate → 1-Tert-butoxycarbonylamino-2-(2-methylsulfanylethyl)cyclopropanecarboxylic acid methyl ester

https://huagongshe.com/reaction/1893664

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium methanethiolateHCID 4378561—
反応物1-Tert-butoxycarbonylamino-2-(2-methanesulfonyloxyethyl)cyclopropanecarboxylic acid methyl esterHCID 57445167—
溶媒MethanolHCID 887—
生成物1-Tert-butoxycarbonylamino-2-(2-methylsulfanylethyl)cyclopropanecarboxylic acid methyl esterHCID 6861679079%

反応手順

A solution of 1-tert-butoxycarbonylamino-2-(2-methanesulfonyloxyethyl)cyclopropanecarboxylic acid methyl ester (0.52 g, 1.53 mmol) in 5 mL MeOH was added dropwise to a rt solution of sodium thiomethoxide in 3 mL MeOH. After 4.75 h, the solvent was removed in vacuo and the residue was taken up in EtOAc and H2O (15 mL each). The aqueous layer was extracted with 3×10 mL EtOAc. The combined organics were washed with brine and dried over anhydrous MgSO4. Following concentration in vacuo, 1-tert-butoxycarbonylamino-2-(2-methylsulfanylethyl)cyclopropanecarboxylic acid methyl ester (0.350 g, 79%) was obtained as a colorless oil that was used without further purification. LCMS found 312.0 [M+Na]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08513186B2
出典データセットuspto-grants-2013_08
ORD IDord-5865f5aa0b53420c8afd168eb37b20fb
出典メモuspto-grants-2013_08