Water → 1-Methyl-3-(1-methylethoxy)-5-(phenylmethoxy)-1H-indole-2-carboxylic acid

HRID 21587

반응식

HRID 21587 반응식
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:8][CH:9]=2)[C:4]([O:19][CH:20]([CH3:22])[CH3:21])=[C:3]1[C:23]([O:25]C(C)(C)C)=[O:24].[OH-].[Na+].O>COCCO>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][C:7]([O:11][CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)=[CH:8][CH:9]=2)[C:4]([O:19][CH:20]([CH3:22])[CH3:21])=[C:3]1[C:23]([OH:25])=[O:24]

참가 물질

5

반응물 3

HCID 962Water2회HCID 14798Sodium HydroxideHCID 108345245-Benzyloxy-3-isopropoxy-1-methyl-1H-indole-2-carboxylic acid tert-butyl ester

생성물 1

HCID 105690841-Methyl-3-(1-methylethoxy)-5-(phenylmethoxy)-1H-indole-2-carboxylic acid수율 88.4%

시약·촉매·용매 1

HCID 80192-Methoxyethanol용매

실험 절차

A suspension of 1,1-dimethylethyl 1-methyl-3(1-methylethoxy)-5-(phenylmethoxy)-1H-indole-2-carboxylate (5.6 g, 14 mmol) in 80 mL of 2-methoxyethanol is treated with a solution of 50% aqueous sodium hydroxide (5.0 g, 63 mmol) followed by the addition of 15 mL of water. The mixture is stirred at reflux for 3 hours, then cooled and added to 700 mL of water. The mixture is heated on a hot plate until nearly one phase and filtered hot. The warm filtrate is immediately treated with 50 mL of 4.0N HCl. After cooling to room temperature, followed by 1 hour in an ice bath, the precipitated solid is filtered and washed with 25% methanol in water to give 4.2 g (88%) of product suitable for further synthesis. A sample recrystallized from ethyl acetate-hexane has mp 136° C.-dec.

후처리

  1. temperatureat reflux for 3 hours
  2. temperaturecooled
  3. temperatureThe mixture is heated on a hot plate until nearly one phase
  4. filtrationfiltered hot
  5. additionThe warm filtrate is immediately treated with 50 mL of 4.0N HCl
  6. filtrationthe precipitated solid is filtered
  7. washwashed with 25% methanol in water

출처 및 근거

ORD 기록
ord-9619e7daf99446a5b0dceda6fd6203e7
출처 데이터셋
uspto-grants-1995_06
특허 번호
US05424329

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