참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N-Dimethylaniline | HCID 949 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Benzyl chloroformate | HCID 10387 | — |
| 반응물 | Pyrrolidinone, (4-aminophenyl)- | HCID 676146 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Benzyl 4-(2-oxo-1-pyrrolidinyl)phenylcarbamate | HCID 7686496 | 73.8% |
반응 단계
4.27 g (25.03 mmol) of benzyl chloroformate are slowly added to 4 g (22.7 mmol) of 1-(4-aminophenyl)pyrrolidin-2-one and 3.6 ml (28.4 mmol) of N,N-dimethylaniline in 107 ml of tetrahydrofuran at −20° C. The mixture is stirred at −20° C. for 30 minutes and then allowed to reach room temperature. 0.5 l of ethyl acetate is added, and the organic phase is washed with 0.5 l of saturated NaCl solution. The removed organic phase is dried with MgSO4, and the solvent is evaporated in vacuo. The residue is triturated with diethyl ether and filtered off with suction. 5.2 g (73.8% of theory) of benzyl 4-(2-oxo-1-pyrrolidinyl)phenylcarbamate are obtained as pale beige crystals with a melting point of 174° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07767702B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-b678ad7d47524d1ab57465d1e6ea7d61 |
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| 출처 메모 | uspto-grants-2010_08 |
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