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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 504273생성일: 2026년 10월 25일

1-Benzyl-3-pyrrolidinone → HCID 66661626, 화합물

https://huagongshe.com/reaction/504273

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참여 물질

역할이름HCID투입량
반응물1-Benzyl-3-pyrrolidinoneHCID 69890—
반응물N-(1,1-Dimethylethyl)benzenesulfonamideHCID 314059—
반응물HCID 178418306HCID 178418306—
용매Diethyl EtherHCID 3283—
용매PentaneHCID 8003—
생성물HCID 66661626HCID 6666162639.5%

반응 조건

온도-78 °C

반응 단계

To a solution of N-(tert-butyl)benzenesulfonamide (536 mg, 0.00251 mol) in ether (10 mL, 0.1 mol) was added 1.7 M of tert-butyllithium in pentane (4.4 mL) under nitrogen at −78° C. The mixture was stirred at −78 Celsius for 15 min, then at 0 Celsius for 1 hour, and then cooled down to −78 Celsius again. A solution of 1-benzylpyrrolidin-3-one (400.0 mg, 0.002283 mol) in ether (3 mL) was added to the above solution. The reaction solution was stirred at ±78 Celsius for 2 hours, then quenched with saturated NH4Cl aqueous solution, and then extracted with EtOAc. The organic phase was washed with brine, then dried over MgSO4. The residue was purified by flash chromatography on silica gel column with 30% AcOEt in hexanes to give the desired compound (350 mg, 39% yield). MS (ESI): 389.1 (M+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07776874B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-38a87060dc734d9e96bdeea77f1db806
출처 메모uspto-grants-2010_08