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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20910생성일: 2026년 10월 24일

Acetic Acid → 1-(6-Benzyloxycarbonylamino-hexanoyl)-4-oxo-pyrrolidine-3-carboxylic Acid Ethyl Ester

https://huagongshe.com/ko/reaction/20910

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Potassium tert-butoxideHCID 23665647—
반응물HCID 57834643HCID 57834643—
용매TolueneHCID 1140—
생성물1-(6-Benzyloxycarbonylamino-hexanoyl)-4-oxo-pyrrolidine-3-carboxylic Acid Ethyl EsterHCID 68637397—

반응 조건

온도0 °C

반응 단계

To a suspension of potassium t-butoxide (7.12 g, 64 mmol) in toluene (150 mL) at 0° C. under nitrogen, was added diester 59 (20 g, 44 mmol) in toluene (25 mL) over a 10 min period. The solution was stirred for 30 min at 0° C. and 5 mL of glacial acetic acid was added, immediately followed by 25 g of NaH2PO4.H2O in 250 mL of ice-cold water. The resultant mixture was extracted with chloroform (3×200 mL), and the combined organic extracts were washed twice with phosphate buffer (2×25 mL, pH=7.0), dried over anhydrous sodium sulfate and evaporated to dryness. The residue was dissolved in toluene (300 mL), cooled to 0° C., and extracted with cold pH 9.5 carbonate buffer (3×150 mL). The aqueous extracts were converted to pH 3 with phosphoric acid, and extracted with chloroform (5×125 mL) which were combined, dried, and evaporated to a afford keto ester 60 (12 g, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745608B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b52b11e75f354ffb8e94fc7089281b49
출처 메모uspto-grants-2010_06