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HRID 22679作成日:2026年10月25日

Diethyl Ether → 1-Benzyl 2-(tert-butyl) 4-hydroxypyrazolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/22679

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物1-Benzyl 2-tert-butyl 4-oxopyrazolidine-1,2-dicarboxylateHCID 20724755—
溶媒TetrahydrofuranHCID 8028—
生成物1-Benzyl 2-(tert-butyl) 4-hydroxypyrazolidine-1,2-dicarboxylateHCID 2072475393%

反応条件

温度-78 °C

反応手順

4-Oxo-pyrazolidine-1,2-dicarboxylic acid 1-benzyl ester 2-tert-butyl ester, 27, (5.0 g, 15.6 mmol) is dissolved in tetrahydrofuran (150 mL) and the solution cooled to −78° C. A 5.0 M solution of borane-dimethyl sulfide complex in ether (6.24 mL, 31.2 mmol) is added dropwise via syringe. After 40 minutes at −78° C., the reaction is quenched by slow addition of a saturated aqueous solution of ammonium chloride (20 mL) The cooling bath is removed, and the mixture allowed to warm to ambient temperature with vigorous stirring. The solvent is removed in vacuo and the residue diluted with dichloromethane (200 mL). The mixture is washed with water (150 mL) and saturated aqueous sodium bicarbonate solution (150 mL), water and brine. The combined aqueous layers are extracted with dichloromethane (200 mL), water (150 mL), NaCl (sat.) (200 mL), dried over sodium sulfate, filtered and concentrated in vacuo to afford 4.66 g (93% yield) of the desired product as a clear, viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06849627B2
出典データセットuspto-grants-2005_02
ORD IDord-8fd396eb07384b19b02d269c9665c82c
出典メモuspto-grants-2005_02