Dichloromethane → 1,3-Benzodioxole, 5-methyl-

HRID 395253

反応式

HRID 395253 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([OH:9])[C:5](=[CH:7][CH:8]=1)[OH:6].[OH-].[Na+].[CH2:12](Cl)Cl>C(OCC)(=O)C>[CH2:12]1[O:6][C:5]2[CH:7]=[CH:8][C:2]([CH3:1])=[CH:3][C:4]=2[O:9]1

参加物

5

反応物 3

HCID 6344DichloromethaneHCID 99584-MethylcatecholHCID 14798Sodium Hydroxide

生成物 1

HCID 815641,3-Benzodioxole, 5-methyl-収率 71.9%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
100 °C

実験手順

A mixture of 4-methylcatechol (26.0 g, 209.4 mmol) and NaOH (18.4 g, 461.0 mmol) in CH2Cl2 (40.0 mL) was heated to 100° C. under nitrogen for 2 hours. The solution was allowed to cool to ambient temperature and diluted with ethyl acetate (500 mL). The mixture was washed with NaHCO3 (200 mL) and H2O (2×200 mL). The organic layer was dried over Na2SO4, filtered and concentrated to give a crude oil. Flash chromatography eluting with hexane (100%) gradient to ether/hexane (1:1) afforded the title intermediate as a colorless oil 20.5 g (71.9%).

後処理

  1. temperatureto cool to ambient temperature
  2. washThe mixture was washed with NaHCO3 (200 mL) and H2O (2×200 mL)
  3. dry with materialThe organic layer was dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customto give a crude oil
  7. washFlash chromatography eluting with hexane (100%) gradient to ether/hexane (1:1)

出典と根拠

ORDレコード
ord-07f0cc7de98e4b4aa8fd7d1923e436ad
出典データセット
uspto-grants-2003_08
特許番号
US06605596B2

関連ノート

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