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Tributylvinyltin → 2-Methoxy-7-vinyl-naphthalene

HRID 1825045
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인쇄 미리보기

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HRID 1825045 반응식
[Li+].[Cl-].[CH3:3][O:4][C:5]1[CH:14]=[C:13]2[C:8]([CH:9]=[CH:10][C:11](OS(C(F)(F)F)(=O)=O)=[CH:12]2)=[CH:7][CH:6]=1.[CH2:23]([Sn](CCCC)(CCCC)C=C)[CH2:24]CC>Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[CH3:3][O:4][C:5]1[CH:6]=[CH:7][C:8]2[C:13](=[CH:12][C:11]([CH:23]=[CH2:24])=[CH:10][CH:9]=2)[CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 81998TributylvinyltinHCID 433294Lithium ChlorideHCID 10892112Methanesulfonic acid, trifluoro-, 7-methoxy-2-naphthalenyl ester

생성물 1

HCID 221449672-Methoxy-7-vinyl-naphthalene수율 97.8%

시약·촉매·용매 1

HCID 178418476HCID 178418476, 화합물촉매

반응 조건

온도
90 °C

실험 절차

To a mixture of (Ph3P)2PdCl2 (1.752 g), LiCl (6.36 g), and trifluoromethanesulfonic acid 7-methoxy-naphthalen-2-yl ester (15.3 g) was added dropwise tributyl(vinyl)tin (19.02 g). The resulting mixture was stirred over 4 h at 90° C. The reaction was quenched with water and extracted with CH2Cl2. The organic layer was washed with water and dried over MgSO4. After concentration, the crude product was purified by flash chromatography eluting with 20% ethyl acetate in hexanes to give the title compound as an oil (9 g).

후처리

  1. customThe reaction was quenched with water
  2. extractionextracted with CH2Cl2
  3. washThe organic layer was washed with water
  4. dry with materialdried over MgSO4
  5. concentrationAfter concentration
  6. customthe crude product was purified by flash chromatography
  7. washeluting with 20% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-ef4095385e1d466d89f26722f924be1f
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045551B2

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