Dimethyl Sulfate → 1,3-Dihydro-4-methoxy-1,3-dimethyl-2H-indol-2-one

HRID 1090066노트

반응식

HRID 1090066 반응식
[OH:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]([CH3:13])[C:5](=[O:12])[N:6]2[CH3:11].[C:14](=O)([O-])[O-].[K+].[K+].COS(OC)(=O)=O>CC(C)=O>[CH3:14][O:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]([CH3:13])[C:5](=[O:12])[N:6]2[CH3:11]

참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 196929451,3-dihydro-4-hydroxy-1,3-dimethyl-2H-indol-2-one

생성물 1

HCID 196929551,3-Dihydro-4-methoxy-1,3-dimethyl-2H-indol-2-one수율 86.2%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A slurry of 1,3-dihydro-4-hydroxy-1,3-dimethyl-2H-indol-2-one (50 g), milled potassium carbonate (60.1 g) and HPLC grade acetone (400 ml) was mechanically stirred at room temperature as dimethylsulfate (41.4 ml) was added dropwise. The addition funnel was replaced with a condenser and the slurry was refluxed for 18 hours. The K2CO3 was filtered off and washed well with acetone. Acetone was evaporated and the residue was purified by column chromatography to yield 46.5 g of an oil. The oil was dissolved in ether and placed in the refrigerator where, upon standing overnight, the product crystallized, m.p. 73°-74° C.

후처리

  1. additionwas added dropwise
  2. customThe addition funnel was replaced with a condenser
  3. temperaturethe slurry was refluxed for 18 hours
  4. filtrationThe K2CO3 was filtered off
  5. washwashed well with acetone
  6. customAcetone was evaporated
  7. customthe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-86cb37c8d97842b4942ca9b1ae9a5a60
출처 데이터셋
uspto-grants-1992_01
특허 번호
US05081117

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