戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 492049作成日:2026年10月24日

1-Aminocyclopropane-1-carboxylic acid → 1-[(1-Cyclohexylcarbonyloxy-2-methylpropoxy)carbonylamino]cyclopropanecarboxylic Acid

https://huagongshe.com/ja/reaction/492049

反応式

関与物質

役割名称HCID仕込み量
反応物1-Aminocyclopropane-1-carboxylic acidHCID 535—
反応物1-(2,5-Dioxoazolidinyloxycarbonyloxy)-2-methylpropyl cyclohexanecarboxylateHCID 86610293—
溶媒Acetonitrile--water (1/1)HCID 18373917—
生成物1-[(1-Cyclohexylcarbonyloxy-2-methylpropoxy)carbonylamino]cyclopropanecarboxylic AcidHCID 2479840727%

反応手順

Following the general procedure for the synthesis of acyloxyalkyl carbamates, ACPC (0.533 g, 5.27 mmol) and 1-(2,5-dioxoazolidinyloxycarbonyloxy)-2-methylpropyl cyclohexanecarboxylate (1.5 g, 4.39 mmol) were reacted in the acetonitrile/water mixture to provide 0.368 g (27% yield) of the title compound (11) as a white powder after work-up and mass-guided preparative HPLC purification. M.p.: 156-158.5° C. 1H NMR (CDCl3, 400 MHz): δ=6.59 (d, 1H), 6.05 (br s, 0.3H), 5.41 (s, 0.7H), 2.38 (m, 1H), 2.13 (m, 1H), 1.96 (d, 2H), 1.78 (m, 2H), 1.6 (m, 3H), 1.44 (m, 2H), 1.23 (m, 5H), 0.99 (m, 6H). MS (ESI) m/z 350.05 (M+Na)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531572B2
出典データセットuspto-grants-2009_05
ORD IDord-8618fd98246145c5ae8593ae8c6eb135
出典メモuspto-grants-2009_05