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Water → Methyl 3-methyl-1-{3-(phenyl)propyl}-1H-indole-6-carboxylate

HRID 392218
ノート
印刷プレビュー

反応式

HRID 392218 の反応式
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([O:13][CH3:14])=[O:12])=[CH:8][CH:9]=2)[NH:4][CH:3]=1.Br[CH2:16][CH2:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[OH-].[Na+].O>CC(C)=O>[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([O:13][CH3:14])=[O:12])=[CH:8][CH:9]=2)[N:4]([CH2:16][CH2:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 12503(3-Bromopropyl)benzeneHCID 14798Sodium HydroxideHCID 21938240Methyl 3-methyl-1H-indole-6-carboxylate

生成物 1

HCID 22663283Methyl 3-methyl-1-{3-(phenyl)propyl}-1H-indole-6-carboxylate収率 71.4%

試薬・触媒・溶媒 1

HCID 180Acetone
溶媒

実験手順

A stirred solution of methyl 3-methyl-1H-indole-6-carboxylate (0.5 g, Reference Example 30) in acetone (35 ml) was treated with 1-bromo-3-phenylpropane (0.577 g) and sodium hydroxide (0.116 g). The mixture was stirred at room temperature for 12 hours then poured into water (35 ml) and then extracted three times with ethyl acetate (50 ml). The combined extracts were washed with dilute hydrochloric acid (50 ml, 1N) then with saturated sodium bicarbonate solution (50 ml), then dried over magnesium sulphate and then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and hexane (50:1, v/v) to yield the title compound (0.58 g).

後処理

  1. extractionextracted three times with ethyl acetate (50 ml)
  2. washThe combined extracts were washed with dilute hydrochloric acid (50 ml, 1N)
  3. dry with materialwith saturated sodium bicarbonate solution (50 ml), then dried over magnesium sulphate
  4. customevaporated
  5. additionThe residue was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and hexane (50:1

出典と根拠

ORDレコード
ord-cf19aed7c5ba4e4588005a85384c3bfe
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06800645B1

反応ノート

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