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HRID 223319作成日:2026年10月26日

Water → N-Boc-1-fluoropent-4-EN-2-amine

https://huagongshe.com/reaction/223319

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TriethylamineHCID 8471—
反応物2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
反応物1-Fluoropent-4-EN-2-amine hclHCID 20508329—
溶媒TetrahydrofuranHCID 8028—
生成物N-Boc-1-fluoropent-4-EN-2-amineHCID 2050833785%

反応手順

Tert-Butoxycarbonyloxyimino-2-phenylacetonitrile (3.34 g, 13.6 mmoles) in dry tetrahydrofuran (40 ml) is slowly added with ice cooling to a stirred mixture of 1-fluoro-2-amino-4pentene hydrochloride (1.9 g, 13.6 mmoles) prepared in Example 2 and triethylamine (2.78 g, 27.2 mmoles) in tetrahydrofuran (30 ml). After standing overnight (about 16 hours) at room temperature, water is added, the tetrahydrofuran is removed under reduced pressure, and the residue is extracted twice with ether. After washing with 1 N sodium hydroxide, then with water until neutral, the organic layer is dried and concentrated at reduced pressure to give 1-fluoro-2-tert-butoxycarbonylamino-4-pentene (2.33 g, 85%) as an oil which is used in Example 4 without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04353828
出典データセットuspto-grants-1982_10
ORD IDord-19fabd3244a94c2db74dc639067bb9fb
出典メモuspto-grants-1982_10