참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | N-[(Trimethylsilyl)methyl]benzylamine | HCID 353458 | — |
| 반응물 | Diethyl fumarate | HCID 638144 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | diethyl (3S,4S)-1-benzylpyrrolidine-3,4-dicarboxylate | HCID 6558921 | — |
반응 단계
900 g of N-Benzyl-N-trimethylsilylmethyl-amine (4654 mmol) were dissolved in 5.6 l THF at 20-25° C. 450 ml of 36% aqueous formaldehyde (5880 mmol, 1.26 equiv.) were added over 15 min, keeping the temperature between 20-25° C. After 15 min, a mixture of 760 ml diethyl fumarate (1 equiv.), 2.25 l THF and 11.2 ml trifluoroacetic acid (0.03 equiv.) was added over 15 min. The reaction mixture was stirred overnight keeping the temperature between 20-30° C. (in process control by GC). 3.5 l of 1N HCl were added, followed by 2.3 l heptane. The aqueous phase was separated and washed with 3.4 l heptane. The heptane phases were washed sequentially with 3.5 l 1N HCl. 4.5 l MTBE were added to the combined aqueous phases. 720 ml of 32% NaOHaq were added (pH 13) under vigorous stirring. The aqueous phase was separated and re-extracted with 4.5 l MTBE. The MTBE phases were washed sequentially with 2.2 l water, combined and concentrated to dryness at 45° C. to give 1.295 kg of crude (rac)-trans-N-benzyl-pyrrolidine-3,4-dicarboxylic acid diethyl ester. If required, the crude cycloadduct can be distilled.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07872141B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-56aeac7bf4a1403291318c15e82a0b8b |
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| 출처 메모 | uspto-grants-2011_01 |
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