Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17617생성일: 2026년 10월 24일
Allyl Alcohol → 2-Cyclopropyl-7-(1-hydroxymethylvinyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile
https://huagongshe.com/ko/reaction/17617
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Allyl Alcohol | HCID 7858 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Cyano-2-cyclopropyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl trifluoromethanesulfonate | HCID 86630884 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 촉매 | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-Cyclopropyl-7-(1-hydroxymethylvinyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile | HCID 68584699 | 32.5% |
반응 단계
4-Cyano-2-cyclopropyl-5-methyl-6-phenyl-1,3-benzoxazol-7-yl trifluoromethanesulfonate (I-323) (760 mg, 1.80 mmol) was dissolved in dimethylformamide (10 ml), then triethylamine (276 μl, 1.98 mmol), allyl alcohol (209 mg, 3.60 mmol), 1,1′-bis(diphenylphosphino)ferrocene (79.8 mg, 0.144 mmol) and palladium(II) acetate (24.2 mg, 0.108 mmol) were added, followed by stirring in an oil bath at 100° C. under argon atmosphere for 16 hours. The reaction liquid was concentrated under reduced pressure, the residue was dissolved in ethyl acetate, washed with water and saturated brine. After drying over anhydrous sodium sulfate, the insoluble matter was separated by filtration, and the residue obtained by concentration was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=1:1, v/v) to obtain the entitled compound (193 mg, 32%) as a colorless oily substance.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07737166B2 |
|---|
| 출처 데이터셋 | uspto-grants-2010_06 |
|---|
| ORD ID | ord-fcdca3eeee61483893e9bc63ac311015 |
|---|
| 출처 메모 | uspto-grants-2010_06 |
|---|