홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Dimethyl Sulfoxide → 2-Vinylanisole

HRID 1821658
노트
인쇄 미리보기

반응식

HRID 1821658 반응식
[H-].[Na+].[CH3:3][O:4][C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[CH:7]=O.[CH3:13]S(C)=O>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH3:3][O:4][C:5]1[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=1[CH:7]=[CH2:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 679Dimethyl Sulfoxide2회HCID 86582-MethoxybenzaldehydeHCID 24758Sodium hydride

생성물 1

HCID 611532-Vinylanisole수율 61.1%

시약·촉매·용매 1

HCID 74505Methyltriphenyliphosphonium bromide촉매

반응 조건

온도
85 °C

실험 절차

Under nitrogen atmosphere, in dry dimethylsulfoxide (15 mL) was suspended 1.92 g (48.0 mmol) of 60% sodium hydride washed with hexane, after stirring the suspension at 85° C. for 30 minutes, it was cooled to room temperature and then, in an ice bath, a dry dimethylsulfoxide (35 mL) solution containing 17.2 g (48.2 mmol) of methyl(triphenyl)phosphonium bromide was gradually added dropwise thereto. After stirring at room temperature for 20 minutes, 4.83 mL (40.1 mmol) of commercially available 2-methoxybenzaldehyde was added dropwise thereto, and the resulting mixture was stirred at room temperature for 1 hour and then at 65° C. for 3 hours. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was successively washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed, and the obtained residue was purified by silica gel column chromatography (Wako gel C-100, hexane-ethyl acetate, gradient) to obtain 3.29 g (24.5 mmol, Yield: 61.1%) of 1-methoxy-2-vinylbenzene.

후처리

  1. washwashed with hexane
  2. temperatureit was cooled to room temperature
  3. additionwas gradually added dropwise
  4. stirringAfter stirring at room temperature for 20 minutes
  5. stirringthe resulting mixture was stirred at room temperature for 1 hour
  6. waitat 65° C. for 3 hours
  7. extractionextracted with ethyl acetate
  8. washThe organic layer was successively washed with water and brine
  9. dry with materialdried over anhydrous magnesium sulfate
  10. customThe solvent was removed
  11. customthe obtained residue was purified by silica gel column chromatography (Wako gel C-100, hexane-ethyl acetate, gradient)

출처 및 근거

ORD 기록
ord-dfabc9af3d104b81b5bb0166de1bc63e
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07608563B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트