Catechol → 2,3-Dihydro-2,2-dimethyl-7-benzofuranol

HRID 482804

반응식

HRID 482804 반응식
[C:1]1([C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4])[OH:2].Cl[CH2:10][C:11]([CH3:13])=[CH2:12].[OH-].[Na+].COS([O:21][CH3:22])(=O)=O>O>[CH3:10][C:11]1([CH3:13])[CH2:12][C:8]2[CH:7]=[CH:6][CH:5]=[C:3]([OH:4])[C:1]=2[O:2]1.[CH3:12][C:11]1([CH3:13])[CH2:10][C:8]2[CH:7]=[CH:6][CH:5]=[C:3]([O:21][CH3:22])[C:1]=2[O:2]1

참가 물질

7

반응물 4

HCID 289CatecholHCID 6497Dimethyl SulfateHCID 112413-Chloro-2-methyl-1-propeneHCID 14798Sodium Hydroxide

생성물 2

HCID 152782,3-Dihydro-2,2-dimethyl-7-benzofuranolHCID 135313777-Methoxy-2,2-dimethyl-2,3-dihydro-1-benzofuran

시약·촉매·용매 1

HCID 962Water용매

실험 절차

The starting material 2,3-dihydro-2,2-dimethyl-7-benzofuranol is prepared from catechol and 3-chloro-2-methylpropene as described by Neth. No. 6,500,340. The material (16.4 g) is added to 125 ml of water and contacted with 8 ml of 50% NaOH. After stirring one-half hour, 16.4 g of dimethylsulfate is added and the resulting suspension is stirred and heated at 60° for 2 hours. The resulting mixture is extracted with methylene chloride. The organic phase is dried over sodium sulfate and the solvent is evaporated under reduced pressure. The residual oil is distilled to afford 2,3-dihydro-2,2-dimethyl-7-methoxybenzofuran.

후처리

  1. stirringthe resulting suspension is stirred
  2. temperatureheated at 60° for 2 hours
  3. extractionThe resulting mixture is extracted with methylene chloride
  4. dry with materialThe organic phase is dried over sodium sulfate
  5. customthe solvent is evaporated under reduced pressure
  6. distillationThe residual oil is distilled

출처 및 근거

ORD 기록
ord-cde4ca8fb730469395b1c40d09defc1a
출처 데이터셋
uspto-grants-1986_03
특허 번호
US04576632

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