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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 497479생성일: 2026년 10월 26일

Cinnamaldehyde → (4R)-4-Benzyl-3-{(2R,3R)-2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-hydroxy-5-phenyl-pent-4-enoyl}-oxazolidin-2-one

https://huagongshe.com/reaction/497479

반응식

참여 물질

역할이름HCID투입량
반응물CinnamaldehydeHCID 637511—
반응물SparteineHCID 644020—
반응물(R)-4-Benzyl-3-[5-(tert-butyl-diphenyl-silanyloxy)-pentanoyl]-oxazolidin-2-oneHCID 59094988—
촉매Titanium TetrachlorideHCID 24193—
용매DichloromethaneHCID 6344—
생성물(4R)-4-Benzyl-3-{(2R,3R)-2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-hydroxy-5-phenyl-pent-4-enoyl}-oxazolidin-2-oneHCID 6974783983.2%

반응 단계

To a stirring solution of (R)-4-benzyl-3-[5-(tert-butyl-diphenyl-silanyloxy)-pentanoyl]-oxazolidin-2-one (1.64 g, 3.19 mmol) in dry methylene chloride (15.9 mL) in a flame dried round bottom flask under N2 at 0° C. was added titanium(IV) chloride (386 μL, 3.51 mmol). After 5 min, (−)-sparteine (1.83 mL, 7.97 mmol) was added. After 20 min, trans-cinnamaldehyde (442 μL, 3.51 mmol) was added dropwise to the purple suspension, and the resulting pale green-yellow solution was stirred for 1 h. The reaction was quenched by the addition of 50% saturated ammonium chloride (50 mL), diluted with water (100 mL), and then extracted with methylene chloride (3×30 mL). The organic layers were combined, washed with brine, dried over sodium sulfate, and concentrated in vacuo to a colorless oil. The oil was purified by flash chromatography (SiO2, 15-30% ethyl acetate in hexanes) to yield 1.72 g (83.1%) of the desired product as a white solid. MS (APCI), m+/z: (M+H)+=648.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06949546B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-906f29d688e64af9acd4ae62ff716c69
출처 메모uspto-grants-2005_09