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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 971591생성일: 2026년 10월 25일

Tetrahydrofuran → (S)-N-Carbobenzyloxy-3-(3,4-diformyloxyphenyl)-2-methylalanine

https://huagongshe.com/reaction/971591

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Acetic-formic anhydrideHCID 75269—
반응물(2S)-2-{[(benzyloxy)carbonyl]amino}-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acidHCID 18595367—
생성물(S)-N-Carbobenzyloxy-3-(3,4-diformyloxyphenyl)-2-methylalanineHCID 54440584100%

반응 단계

A solution of (S)-N-carbobenzyloxy-3-(3,4-dihydroxyphenyl)-2-methylalanine (0.35 g, 1 mmol) and acetic formic anhydride (0.36 g, 4 mmol) in anhydrous tetrahydrofuran (5 ml) is stirred 24 hours at 20°-25° under dry N2. The solvent is evaporated in vacuo and the residue is dried further at 0.1mm/25° for 2 hours. The product (A) (0.4g, 100%) is obtained as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04160712
출처 데이터셋uspto-grants-1979_07
ORD IDord-3f0910666326437e8a5216fc9950aee0
출처 메모uspto-grants-1979_07