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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253725생성일: 2026년 10월 26일

Hydrochloric Acid → diethyl (3S,4S)-1-benzylpyrrolidine-3,4-dicarboxylate

https://huagongshe.com/reaction/253725

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Trifluoroacetic acidHCID 6422—
반응물N-[(Trimethylsilyl)methyl]benzylamineHCID 353458—
반응물Diethyl fumarateHCID 638144—
용매TetrahydrofuranHCID 8028—
용매HeptaneHCID 8900—
생성물diethyl (3S,4S)-1-benzylpyrrolidine-3,4-dicarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872141B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-56aeac7bf4a1403291318c15e82a0b8b
출처 메모uspto-grants-2011_01