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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cinnamaldehyde | HCID 637511 | — |
| 반응물 | Sparteine | HCID 644020 | — |
| 반응물 | (R)-4-Benzyl-3-[5-(tert-butyl-diphenyl-silanyloxy)-pentanoyl]-oxazolidin-2-one | HCID 59094988 | — |
| 촉매 | Titanium Tetrachloride | HCID 24193 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (4R)-4-Benzyl-3-{(2R,3R)-2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-hydroxy-5-phenyl-pent-4-enoyl}-oxazolidin-2-one | HCID 69747839 | 83.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06949546B2 |
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| 출처 데이터셋 | uspto-grants-2005_09 |
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| ORD ID | ord-906f29d688e64af9acd4ae62ff716c69 |
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| 출처 메모 | uspto-grants-2005_09 |
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