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HRID 12913作成日:2026年10月23日

2-Amino-2-methyl-1-propanol → Tert-butyl 2-(1-hydroxy-2-methylpropan-2-yl)hydrazine-1-carboxylate

https://huagongshe.com/ja/reaction/12913

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-2-methyl-1-propanolHCID 11807—
反応物N-Boc-3-(4-cyanophenyl)oxaziridineHCID 2725038—
溶媒Diethyl EtherHCID 3283—
生成物Tert-butyl 2-(1-hydroxy-2-methylpropan-2-yl)hydrazine-1-carboxylateHCID 5454169440%

反応手順

A solution of N-(tert-butoxycarbonyl)-3-(4-cyanophenyl)-oxaziridine (CAS #: 150884-56-3, purchased from Acros, 5.17 g, 21 mmol) in anhydrous diethyl ether (20 mL) was added to a solution of 2-amino-2-methyl-propan-1-ol (1.78 g, 20 mmol) in anhydrous diethyl ether (20 mL) at room temperature. The reaction mixture stirred at room temperature for 2 hours. Diethyl ether was evaporated under reduced pressure and the residue was purified by flash chromatography eluting with a gradient of 3-5% methanol/dichloromethane to give N′-(2-hydroxy-1,1-dimethyl-ethyl)-hydrazinecarboxylic acid tert-butyl ester (1.63 g, 40%) which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728029B2
出典データセットuspto-grants-2010_06
ORD IDord-279d0f43f58a4171a279e21137b58bb2
出典メモuspto-grants-2010_06