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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132936생성일: 2026년 10월 26일

Hydrogen Peroxide → (S)-2-((R)-3-isopropyl-2-oxopyrrolidin-1-yl)-4-phenylbutanoic acid

https://huagongshe.com/reaction/132936

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Lithium HydroxideHCID 3939—
반응물(R)-2-isopropylpent-4-enoic acidHCID 6915842—
반응물(2R,4R)-tert-butyl 4-(allyloxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 67315914—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(S)-2-((R)-3-isopropyl-2-oxopyrrolidin-1-yl)-4-phenylbutanoic acidHCID 69193934—

반응 조건

온도0 °C

반응 단계

Step D (3): (R)-2-isopropylpent-4-enoic acid. To a solution of the compound of step D (2) (1.08 g, 3.59 mmol) in THF (14.4 mL) was added water (3.59 mL), and the mixture cooled to 0° C. A solution of LiOH (172.5 mg, 7.20 mmol) and 30% H2O2 (3.26 mL) in water (11.2 mL) was added, and the combined mixture stirred for 10 minutes at 0° C. The ice bath was removed, and the reaction was allowed to continue for 1 h at rt. A solution of sodium sulfite (3.63 g) was added, and the reaction stirred for 10 min. Saturated sodium carbonate solution was added, and the reaction was extracted with methylene chloride. The aqueous layer was acidified to pH 1 with 6 N HCl, and extracted 3 times with diethyl ether. The combined ether layers were washed with brine, and dried over MgSO4. The extract was filtered, and concentrated in vacuo to afford the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388007B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-283a997f1521485da8e04a718d140aab
출처 메모uspto-grants-2008_06