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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413403생성일: 2026년 10월 24일

Diisopropylamine → 2-[(1,1-Dimethylethoxy)carbonyl]amino-3-phenylmethoxy-4pentenoic acid

https://huagongshe.com/ko/reaction/413403

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물TetrahydrofuranHCID 8028—
반응물Lithium diisopropylamideHCID 2724682—
반응물N-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl esterHCID 69891095—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
용매HexaneHCID 8058—
생성물2-[(1,1-Dimethylethoxy)carbonyl]amino-3-phenylmethoxy-4pentenoic acidHCID 23508263—

반응 단계

A lithium diisopropylamide solution (37.3 M) is prepared from N,N-diisopropylamine (5.2 mL, 37.2 mmol) in THF (30 mL. cooled to −20° C.) and 3.7 mL (37.3 mmol) 10 M n-BuLi in hexane. The LDA solution in THF is added to a stirred solution of N-[(1,1-dimethylethoxy)carbonyl]glycine-4-phenylmethoxy-2-butenyl ester 63a (14.9 mmol) and ZnCl2 (17.9 mmol) in 100 mL THF at −78° C. The mixture is allowed to come to room temperature overnight. The crude mixture is partitioned between 700 mL ethyl acetate and 700 mL 1 N HCl. The organic layer is washed with 150 mL dilute NaHCO3 solution (3×'s). The bicarbonate washes are acidified with conc. HCl to pH1 and extracted with 700 mL ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate and the solvent removed in vacuo to give the named compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06566381B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-6de3ff56f63c420ca8f09f42aad1a704
출처 메모uspto-grants-2003_05