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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 3-Ethyl-6-(methyloxy)-2-phenyl-1-naphthalenyl acetate

HRID 1992851
ノート
印刷プレビュー

反応式

HRID 1992851 の反応式
[CH2:1]([CH:3]1[CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:13][CH3:14])[CH:10]=2)[C:5](=[O:15])[CH:4]1[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[CH3:2].ClC1C(=O)C(C#N)=[C:26](C#N)[C:27](=[O:30])C=1Cl>C(OC(C)=C)(=O)C.C(Cl)Cl>[C:27]([O:15][C:5]1[C:6]2[C:11](=[CH:10][C:9]([O:13][CH3:14])=[CH:8][CH:7]=2)[CH:12]=[C:3]([CH2:1][CH3:2])[C:4]=1[C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1)(=[O:30])[CH3:26]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 685413613-Ethyl-6-(methyloxy)-2-phenyl-3,4-dihydro-1(2H)-naphthalenone

生成物 1

HCID 685362503-Ethyl-6-(methyloxy)-2-phenyl-1-naphthalenyl acetate収率 64%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 7916Isopropenyl acetate溶媒

実験手順

3-Ethyl-6-(methyloxy)-2-phenyl-3,4-dihydro-1(2H)-naphthalenone (55) (0.84 g, 3.00 mmol) was dissolved in isopropenyl acetate (30 mL). pTsOH monohydrate (100 mg) was added. The mixture was refluxed under nitrogen for 3 days. Cooled to room temperature, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (1.74 g, 7.50 mmol) was added. The resulting mixture was refluxed under nitrogen overnight. Cooled to room temperature and diluted with CH2Cl2 (150 mL). The mixture was washed with 0.2 N NaOH (4×20 mL), water (2×20 mL), brine (30 mL), dried over Na2SO4, filtered, and the filtrate was concentrated to give the crude product as a dark brown tar. The crude product was purified by flash chromatography over SiO2 with hexanes:acetone (50:1) to give 0.61 g (64%) of the title compound (56) as a white solid. 1H NMR (400 MHz, CDCl3): δ 1.11 (t, J=7.5 Hz, 3H), 1.97 (s, 3H), 2.55 (q, J=7.5 Hz, 2H), 3.93 (s, 3H), 7.10-7.16 (m, 2H), 7.20-7.25 (m, 2H), 7.30-7.45 (m, 3H), 7.57 (s, 1H), 7.62 (d, J=8.9 Hz, 1H).

後処理

  1. temperatureThe mixture was refluxed under nitrogen for 3 days
  2. temperatureThe resulting mixture was refluxed under nitrogen overnight
  3. temperatureCooled to room temperature
  4. washThe mixture was washed with 0.2 N NaOH (4×20 mL), water (2×20 mL), brine (30 mL)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationthe filtrate was concentrated
  8. customto give the crude product as a dark brown tar
  9. customThe crude product was purified by flash chromatography over SiO2 with hexanes:acetone (50:1)

出典と根拠

ORDレコード
ord-726360292c9d4e7cb423249c60297b37
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07649093B2

反応ノート

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