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Potassium Carbonate → Benzyl 4-{(E)-2-[4-((E)-2-methoxycarbonylvinyl)-2,6-dimethylphenyl]-vinyl}-3-nitrobenzoate

HRID 1360786
ノート
印刷プレビュー

反応式

HRID 1360786 の反応式
[CH2:1]([O:8][C:9](=[O:21])[C:10]1[CH:15]=[CH:14][C:13]([CH2:16]Br)=[C:12]([N+:18]([O-:20])=[O:19])[CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:22]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.COC1C=CC(NC2OC(C3C=CC4N=[C:61]([C:63]5[C:68]([CH3:69])=[CH:67][C:66]([CH2:70][CH2:71][C:72]([OH:74])=[O:73])=[CH:65][C:64]=5[CH3:75])NC=4C=3)=NN=2)=CC=1.C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C.C(OCC)(=O)C>[CH3:22][O:74][C:72](/[CH:71]=[CH:70]/[C:66]1[CH:67]=[C:68]([CH3:69])[C:63](/[CH:61]=[CH:16]/[C:13]2[CH:14]=[CH:15][C:10]([C:9]([O:8][CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)=[O:21])=[CH:11][C:12]=2[N+:18]([O-:20])=[O:19])=[C:64]([CH3:75])[CH:65]=1)=[O:73]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 11430Potassium CarbonateHCID 11776TriphenylphosphineHCID 252354053-(4-{6-[5-(4-Methoxyphenylamino)-[1,3,4]oxadiazol-2-yl]-1H-benzoimidazol-2-yl}-3,5-dimethylphenyl)-propionic acidHCID 66965750Benzyl 4-bromomethyl-3-nitrobenzoate

生成物 1

HCID 66966058Benzyl 4-{(E)-2-[4-((E)-2-methoxycarbonylvinyl)-2,6-dimethylphenyl]-vinyl}-3-nitrobenzoate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
100 °C

実験手順

A mixture of 4-bromomethyl-3-nitrobenzoic acid benzyl ester (2.06 g, 5.88 mmol) and triphenylphosphine (1.54 g, 5.87 mmol) in DMF (10 mL) was heated at 100° C. for 1 h. To this solution was then added 3-(4-formyl-3,5-dimethylphenyl)-acrylic acid methyl ester (1.28 g, 5.86 mmol) (Example 1-60, step C) and potassium carbonate (1.63 g, 11.8 mmol) and the mixture was stirred for at 100° C. 18 h. The mixture was poured into ethyl acetate and extracted with water once and brine five times. The organic layer was dried, filtered, and solvent removed under reduced pressure. The residue was purified by chromatography using a 0-40% gradient of heptane/ethyl acetate to give the title compound.

後処理

  1. custom18 h
  2. extractionextracted with water once
  3. customThe organic layer was dried
  4. filtrationfiltered
  5. customsolvent removed under reduced pressure
  6. customThe residue was purified by chromatography

出典と根拠

ORDレコード
ord-9733602ce9984c9cb99e18d0bbf26487
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07879850B2

反応ノート

読み込み中…

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