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Sodium Hydroxide → HCID 86691639、化合物

HRID 2204023
ノート
印刷プレビュー

反応式

HRID 2204023 の反応式
[OH-].[Na+].[N:3]1([CH:8]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:9][CH2:10][CH2:11][CH2:12][C:13]([O:15]C)=[O:14])[CH:7]=[CH:6][N:5]=[CH:4]1>CO.O>[N:3]1([CH:8]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14])[CH:7]=[CH:6][N:5]=[CH:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14798Sodium HydroxideHCID 86691638HCID 86691638、化合物

生成物 1

HCID 86691639HCID 86691639、化合物収率 77%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

Sodium hydroxide (0.11 g, 2.75 mmol) was added to a stirred solution of methyl 6-(1H-imidazol-1-yl)octadecanoate (0.5 g, 1.37 mmol) in a mixture of methanol (9 ml) and water (3 ml) at 0° C., warmed to room temperature, and stirring continued for another 3 hours. Methanol was removed from the mixture by evaporation. The aqueous layer was acidified with 1N HCl up to pH 4, extracted with dichloromethane (3×15 ml), and the combined organic layers were washed with brine solution, dried on anhydrous MgSO4, and concentrated. Crude product was purified on silica gel column (5% methanol in dichloromethane) to obtain a gummy liquid (370 mg, 77%).

後処理

  1. customMethanol was removed from the mixture by evaporation
  2. extractionextracted with dichloromethane (3×15 ml)
  3. washthe combined organic layers were washed with brine solution
  4. dry with materialdried on anhydrous MgSO4
  5. concentrationconcentrated
  6. customCrude product was purified on silica gel column (5% methanol in dichloromethane)

出典と根拠

ORDレコード
ord-a6a2b4cab7d74acda1ce4b4658d3f2f4
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09365597B2

反応ノート

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