돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 408620생성일: 2026년 10월 25일

Acetic Acid → 1-Benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/408620

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물2-[Benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl esterHCID 70557779—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-2-methyl-azetidine-2-carboxylic acid ethyl esterHCID 7055865879.1%

반응 조건

온도-76 °C

반응 단계

A solution of 2-[benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester (27.4 g, 1 eq.) in 253 mL of dry THF was cooled to −78° C. under argon. KHMDS (15% w/w in toluene, 170.40 g, 1.25 eq.) was slowly added so that temperature was kept below −76° C. The reaction was stirred for 1 h at −76° C., then warmed to 20° C. and stirred for 1 h. Acetic acid (1.74 mL, 0.3 eq.) was added and the reaction was stirred at 20° C. for 10 min. The reaction was quenched with 50 mL of a saturated aqueous solution of NaHCO3 and partially concentrated under reduced pressure. The crude was extracted three times with DCM. The organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc 100/0 to 90/10) to afford 1-benzyl-2-methyl-azetidine-2-carboxylic acid ethyl ester (18.75 g, yield=79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759334B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-65c762b0dd89495094b35cd4931ca45d
출처 메모uspto-grants-2014_06