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Hydrochloric Acid → HCID 86645784、化合物

HRID 1047394
ノート
印刷プレビュー

反応式

HRID 1047394 の反応式
[H-].[Na+].[CH2:3]([OH:25])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24].[Br: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]Br.Cl>CCCCCC.C1(C)C=CC=CC=1>[CH2:3]([O:25][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][Br:26])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 12620Behenyl AlcoholHCID 187661,12-DibromododecaneHCID 24758Sodium hydride

生成物 1

HCID 86645784HCID 86645784、化合物収率 78%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒
HCID 8058
Hexane
溶媒

反応条件

温度
85 °C

実験手順

Sodium hydride (60%, 0.98 g, 24.5 mmol) washed with hexane was suspended in toluene (16 ml), 1-docosanol (4.00 g, 12.2 mmol) was added, 1,12-dibromododecane (8.04 g, 24.5 mmol) was added, and the mixture was stirred at 85° C. for 2 days. The reaction mixture was cooled to room temperature, 1N hydrochloric acid (30 ml) was added dropwise thereto in a water bath to quench the reaction. The mixture was extracted with chloroform (100 ml), and washed 3 times with 1N hydrochloric acid (30 ml), 3 times with 5% aqueous sodium hydrogen carbonate solution (30 ml), and once with 20% aqueous sodium chloride solution (30 ml). The organic layer was dried over sodium sulfate, and the solvent of the filtrate was evaporated. The residue was isolated and purified by silica gel column chromatography and precipitated with methanol (70 ml) to give 12-docosyloxy-dodecyl bromide (yield 78%).

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customin a water bath to quench
  3. customthe reaction
  4. extractionThe mixture was extracted with chloroform (100 ml)
  5. washwashed 3 times with 1N hydrochloric acid (30 ml), 3 times with 5% aqueous sodium hydrogen carbonate solution (30 ml)
  6. dry with materialThe organic layer was dried over sodium sulfate
  7. customthe solvent of the filtrate was evaporated
  8. customThe residue was isolated
  9. custompurified by silica gel column chromatography
  10. customprecipitated with methanol (70 ml)

出典と根拠

ORDレコード
ord-0e05a56b78f64c13b8e9074a44fb5cee
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569453B2

反応ノート

読み込み中…

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