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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1064949생성일: 2026년 10월 24일

(S)-4-Benzyl-3-(ethoxyacetyl)oxazolidin-2-one → HCID 69279901, 화합물

https://huagongshe.com/ko/reaction/1064949

반응식

참여 물질

역할이름HCID투입량
반응물(S)-4-Benzyl-3-(ethoxyacetyl)oxazolidin-2-oneHCID 10825429—
반응물4-Benzyloxy-2-(trifluoromethyl)benzaldehydeHCID 22273885—
반응물HCID 178418657HCID 178418657—
용매TriethylamineHCID 8471—
생성물HCID 69279901HCID 69279901—

반응 단계

In analogy to the procedure described in example 1 a], (S)-4-benzyl-3-ethoxyacetyl-oxazolidin-2-one (for the preparation of (S)-4-benzyl-3-ethoxyacetyl-oxazolidin-2-one see: D. Haigh, H. C. Birrell, B. C. C. Cantello, D. S. Eggleston, R. C. Haltiwanger, R. M. Hindley, A. Ramaswamy, N. C. Stevens, Tetrahedron: Asymmetry 1999, 10, 1353-1367) was reacted with 4-benzyloxy-2-trifluoromethyl-benzaldehyde in the presence of triethylamine and di-n-butylboron triflate to give (S)-4-benzyl-3-[(2S,3R)-3-(4-benzyloxy-2-trifluoromethyl-phenyl)-2-ethoxy-3-hydroxy-propionyl]-oxazolidin-2-one as colorless liquid. According to 1H-NMR spectroscopy, one of the four isomers is strongly predominating. The configuration was tentatively assigned as 2S,3R according to D. Haigh et al., Tetrahedron: Asymmetry 1999, 10, 1353-1367.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06969725B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-5e14ff88f7014ad287707ab08f759c17
출처 메모uspto-grants-2005_11