참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Benzyl-3-pyrrolidinone | HCID 69890 | — |
| 반응물 | N-(1,1-Dimethylethyl)benzenesulfonamide | HCID 314059 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Pentane | HCID 8003 | — |
| 생성물 | HCID 66661626 | HCID 66661626 | 39.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07776874B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-38a87060dc734d9e96bdeea77f1db806 |
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| 출처 메모 | uspto-grants-2010_08 |
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