戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 3374作成日:2026年10月23日

Tetrahydrofuran → N-Methoxy-N-methylcyclopropanecarboxamide

https://huagongshe.com/ja/reaction/3374

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物N-tert-butoxycarbonyl-3-methoxy-2-methylanilineHCID 10609918—
反応物[2-(Tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketoneHCID 10804518—
反応物CID 53628100HCID 178418400—
溶媒CyclohexaneHCID 8078—
生成物N-Methoxy-N-methylcyclopropanecarboxamideHCID 15643267—

反応手順

Using the procedure described in Example 9, Part A, 100 mL (130 mmol) of 1.3M sec-butyl lithium in cyclohexane was reacted with N-tert-butoxycarbonyl-3-methoxy-2-methylaniline (15.4 g, 65 mmol) in 100 mL of THF and then with 8.4 g (65 mmol) of N-methoxy-N-methylcyclopropylcarboxamide to give crude [2-(tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketone. This material on treatment with 20 mL of trifluoroacetic acid in 300 mL of methylene chloride for 6 hours gave a material that was chromatographed on silica gel. Eluting with a gradient, toluene→5% EtOAc/toluene, there was obtained 6.4 g (52% yield) of 2-cyclopropyl-4-methoxy-1H-indole as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733923
出典データセットuspto-grants-1998_03
ORD IDord-34fde6f5003d4e6dab0c33bf86ba9d7f
出典メモuspto-grants-1998_03