Catechol → 2-Ethyl-2-methyl-1,3-benzodioxole

HRID 1030994ノート

反応式

HRID 1030994 の反応式
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].[CH3:9][C:10](=O)[CH2:11][CH3:12].O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O>C(Cl)Cl>[CH2:10]([C:11]1([CH3:12])[O:4][C:3]2[CH:5]=[CH:6][CH:7]=[CH:8][C:1]=2[O:2]1)[CH3:9]

参加物

5

反応物 3

HCID 289CatecholHCID 6569Methyl Ethyl KetoneHCID 14812Phosphorus oxide (P4O10)

生成物 1

HCID 126081602-Ethyl-2-methyl-1,3-benzodioxole収率 58.5%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a stirred solution of 20.0 g (0.180 mole) of catechol and 0.8 g (0.40 mole) of 2-butanone in 200 ml of methylene chloride was added 128.0 g (0.902 mole) of phosphorus pentoxide. The reaction mixture was stirred at room temperature for two days. The stirring was stopped, and the reaction solids were allowed to settle. The reaction mixture was decanted into a separatory funnel. The solid material was washed with methylene chloride, and the wash was decanted into the above separatory funnel. The combined organic phase was washed with aqueous, saturated sodium bicarbonate solution. The washed organic phase was dried over anhydrous magnesium sulfate and was filtered. The filtrate was evaporated under reduced pressure to yield 17.3 g of 2-ethyl-2-methyl-1,3-benzodioxole.

後処理

  1. customthe reaction solids
  2. customThe reaction mixture was decanted into a separatory funnel
  3. washThe solid material was washed with methylene chloride
  4. customthe wash was decanted into the above separatory funnel
  5. washThe combined organic phase was washed with aqueous, saturated sodium bicarbonate solution
  6. dry with materialThe washed organic phase was dried over anhydrous magnesium sulfate
  7. filtrationwas filtered
  8. customThe filtrate was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-a2d51e6699bd44c9950c7af4e032dae7
出典データセット
uspto-grants-1992_04
特許番号
US05108486

反応ノート

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