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HRID 1581534생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1581534

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물1-Benzyl 2-tert-butyl 4-oxopyrazolidine-1,2-dicarboxylateHCID 20724755—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl 2-(tert-butyl) 4-hydroxypyrazolidine-1,2-dicarboxylateHCID 2072475393%

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06730668B2
출처 데이터셋uspto-grants-2004_05
ORD IDord-7586e21a40db43ebb5b8ee6044639131
출처 메모uspto-grants-2004_05