참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Propanol | HCID 1031 | — |
| 반응물 | 1,3-Dichloro-5,5-dimethylhydantoin | HCID 8360 | — |
| 반응물 | Sodium Sulfite | HCID 24437 | — |
| 반응물 | tert-Butyl 2,5-dihydro-1H-pyrrole-1-carboxylate | HCID 5148195 | — |
| 반응물 | N-benzylcarbamate | HCID 22253685 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 생성물 | Tert-butyl 3-(benzyloxycarbonylamino)-4-hydroxy-pyrrolidine-1-carboxylate | HCID 20691380 | — |
반응 단계
N-Propanol (20 ml), benzylcarbamate (4 g, 27 mmol), and 1,3-dichloro-5,5-dimethylhydantoin (2.6 g, 13 mmol) are added to a solution of NaOH (1 g, 27 mmol) in water (40 ml). The reaction mixture is cooled to 0° C. and a solution of 2,5-dihydro-pyrrole-1-carboxylic acid tert-butyl ester (1.51 g, 8.92 mmol) in n-propanol (10 ml) is added. A solution of potassium osmate (0.098 g, 0.268 mmol) in 0.65 M NaOH (1 ml) is added. The reaction mixture is stirred at 0° C. for 1 hour and then at room temperature for 2 hours. The reaction mixture is quenched with sodium sulfite (1.90 g, 15 mmol) and diluted with approximately 1:1 EtOAc:water (100 ml). The aqueous layer is extracted with ethyl acetate, the combined organic extracts dried (MgSO4) and concentrated. Purification on a silica gel column (4:1 hexanes:EtOAc) yields 3-benzyloxycarbonylamino-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07777032B2 |
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| 출처 데이터셋 | uspto-grants-2010_08 |
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| ORD ID | ord-ddaaf293efb845c285160f35a6a0829f |
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| 출처 메모 | uspto-grants-2010_08 |
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