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o-Iodonitrobenzene → 6-(2-Nitrophenyl)-2,3-dimethoxy-7,8-dihydronaphthalene

HRID 1582869
ノート
印刷プレビュー

反応式

HRID 1582869 の反応式
C([O-])(=O)C.[Na+].[CH3:6][O:7][C:8]1[CH:9]=[C:10]2[C:15](=[CH:16][C:17]=1[O:18][CH3:19])[CH:14]=[CH:13][CH2:12][CH2:11]2.I[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=1[N+:27]([O-:29])=[O:28]>CC(N(C)C)=O.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>[N+:27]([C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=1[C:12]1[CH2:13][CH2:14][C:15]2[CH:16]=[C:17]([O:18][CH3:19])[C:8]([O:7][CH3:6])=[CH:9][C:10]=2[CH:11]=1)([O-:29])=[O:28]
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

6

反応物 3

HCID 69115o-IodonitrobenzeneHCID 517045Sodium AcetateHCID 127653926,7-Dimethoxy-3,4-dihydronaphthalene

生成物 1

HCID 227164386-(2-Nitrophenyl)-2,3-dimethoxy-7,8-dihydronaphthalene収率 29%

試薬・触媒・溶媒 2

HCID 178418476HCID 178418476、化合物触媒
HCID 31374
Dimethylacetamide
溶媒

反応条件

温度
140 °C

実験手順

Pd(PPh3)2Cl2 (840 mg, 1.2 mmol) and sodium acetate (200 mg, 2.4 mmol) were added to a solution of 6,7-dimethoxy-3,4-dihydronaphthalene (2, 700 mg, 3.7 mmol) and 1-iodo-2-nitrobenzene (925 mg, 3.7 mmol) in dimethylacetamide (50 mL). The mixture was stirred under nitrogen at 140° C. overnight, and then concentrated in vacuo. Ethyl acetate (60 mL) was added to the residue and washed with distilled water (50 mL). The organic layer was separated and passed through a celite bed. The organic layer was then washed with brine, dried (anhydrous Na2SO4) and concentrated in vacuo. The residue was chromatographed to give compound 3 (330 mg) in 29% yield; 1H NMR (CDCl3) d 2.51(2H, t, J=8.1), 2.92(2H, t, J=8.1), 3.87(3H, s), 3.90(3H, s), 6.45(1H, s), 6.67(1H, s), 6.73(1H, s), 7.38˜7.45 (2H, m), 7.54˜7.62(1H, m), 7.88˜7.93(1H, m); 13C NMR d 28.5, 28.5, 56.6, 111.0, 111.7, 124.9, 127.0, 127.1, 128.1, 128:3, 131.3, 133.3, 135.7, 138.7, 147.9, 148.9.

後処理

  1. concentrationconcentrated in vacuo
  2. additionEthyl acetate (60 mL) was added to the residue
  3. washwashed with distilled water (50 mL)
  4. customThe organic layer was separated
  5. washThe organic layer was then washed with brine
  6. dry with materialdried (anhydrous Na2SO4)
  7. concentrationconcentrated in vacuo
  8. customThe residue was chromatographed

出典と根拠

ORDレコード
ord-360bed0cdf194b48b7a07eaaa8279644
出典データセット
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06740650B2

反応ノート

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