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Methyl iodide → 3-[[6-(2,3-Dihydroxyphenyl)hexyl]oxy]-5-(octadecyloxy)benzoic acid methyl ester

HRID 1492867
ノート
印刷プレビュー

反応式

HRID 1492867 の反応式
[OH:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:17]=[C:18]([CH:22]=[C:23]([O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])[CH:24]=1)[C:19]([OH:21])=[O:20].[C:44](=O)(O)[O-].[Na+].CI>CN(C=O)C>[CH3:44][O:20][C:19](=[O:21])[C:18]1[CH:22]=[C:23]([O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])[CH:24]=[C:16]([O:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([OH:8])[C:2]=2[OH:1])[CH:17]=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 3

HCID 6328Methyl iodide2 回HCID 516892Sodium Bicarbonate2 回HCID 98516283-[[6-(2,3-Dihydroxyphenyl) hexyl]oxy]-5-(octadecyloxy)benzoic acid

生成物 1

HCID 542033863-[[6-(2,3-Dihydroxyphenyl)hexyl]oxy]-5-(octadecyloxy)benzoic acid methyl ester収率 68%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

A mixture of 0.15 g (0.25 mmol) of 3-[[6-(2,3-dihydroxyphenyl) hexyl]oxy]-5-(octadecyloxy)benzoic acid, 0.05 g (0.6 mmol) of sodium bicarbonate and 0.64 ml (10 mmol) of methyl iodide in 3 ml of DMF was stirred and heated at 40° for 5 days. An additional 0.32 ml of methyl iodide and 0.05 g of sodium bicarbonate were added and heating at 40° was continued for 6 days. The solvent was removed at reduced pressure, the residue was extracted with ethyl acetate and the extract was washed with water. The dried extract was concentrated to an oil which was purified by chromatography on 4 g of silica gel using 25% ethyl acetate-hexane to give 0.104 g (68% yield, mp 82°-84°) of 3-[[6-(2,3-dihydroxyphenyl)hexyl]oxy]-5-(octadecyloxy)benzoic acid methyl ester.

後処理

  1. temperatureheated at 40° for 5 days
  2. temperatureheating at 40°
  3. customThe solvent was removed at reduced pressure
  4. extractionthe residue was extracted with ethyl acetate
  5. washthe extract was washed with water
  6. extractionThe dried extract
  7. concentrationwas concentrated to an oil which
  8. customwas purified by chromatography on 4 g of silica gel using 25% ethyl acetate-hexane

出典と根拠

ORDレコード
ord-300fba6623d8429b84a1c8fb19549d50
出典データセット
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05374772

反応ノート

読み込み中…

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