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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1365012생성일: 2026년 10월 26일

Dimethyl Sulfoxide → 1-Benzyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1365012

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물2-Methyl 1-(phenylmethyl) (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylateHCID 688411—
용매DichloromethaneHCID 6344—
용매Ethyl acetate hexaneHCID 21226206—
생성물1-Benzyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylateHCID 1159428870%

반응 단계

To solution of methyl sulfoxide (23.90 ml, 337 mmol) in DCM (100 ml) at −78° C. was added oxalyl chloride (2 M in DCM, 84 ml, 168 mmol) dropwise. The formed solution was stirred at this temperature for 30 min. A solution of (2S,4R)-1-benzyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate (21.38 g, 77 mmol) in DCM (100 ml) was added dropwise at −78° C. The formed slurry was stirred at −78° C. for 2 hr before addition of N,N-Diisopropylethylamine (66.7 ml, 383 mmol) dropwise. The final solution was stirred at room temperature 3 h. The mixture was washed with iced 1M HCl, 5% citric acid, and then brine, dried over MgSO4, filtered, and evaporated. The residual light brown oil was purified by silica gel column chromatography, eluted with 4:1, 3:1, then 2:1 hexane-EtOAc to afford (S)-1-benzyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate (14.8 g, 70% yield) as light brown viscous oil. 1H NMR (CDCl3) δ 2.58-2.63 (m, 1H), 2.90-2.99 (m, 1H), 3.62, 3.77 (s, 3H, rotamers), 3.95-4.02 (m, 2H), 4.82-4.89 (m, 1H), 5.11-5.24 (m, 2H), 7.32-7.39 (m, 5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07888464B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-f7ae63ec81064cb3a1ac362d549927d8
출처 메모uspto-grants-2011_02