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Triethylamine → HCID 86722542、化合物

HRID 1395924
ノート
印刷プレビュー

反応式

HRID 1395924 の反応式
[CH3:1][C:2]([OH:15])([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH3:3].C(N(CC)CC)C.[Br:23][CH:24]([CH3:28])[C:25](Br)=[O:26]>C1(C)C=CC=CC=1>[Br:23][CH:24]([CH3:28])[C:25]([O:15][C:2]([CH3:1])([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH3:3])=[O:26]
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

5

反応物 3

HCID 8471TriethylamineHCID 79047Propanoyl bromide, 2-bromo-HCID 10867656HCID 10867656、化合物

生成物 1

HCID 86722542HCID 86722542、化合物収率 61.27%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
57.5 °C

実験手順

To a stirred solution of 2-methyltridecan-2-ol 73 (5 g, 23.4 mmol) in Toluene (50 mL) was added triethylamine (3.29 mL, 23.4 mmol)) and followed by 2-bromopropionyl bromide 58 (5.11 g, 23.7 mmol) at 5-10° C. The reaction mixture was stirred for 3 hours at 55-60° C.; the reaction was monitored by TLC. The reaction mixture was quenched with saturated sodium bicarbonate solution and stirred for 15 minutes at 25-35° C. The aqueous and organic layers were separated, the organic layer was washed with brine, and the combined organic layers were washed with brine solution. The organic layer was dried over Na2SO4 and concentrated under vacuum to afford crude 74 (5 g, yield: 61.27%) as a liquid.

後処理

  1. customThe reaction mixture was quenched with saturated sodium bicarbonate solution
  2. stirringstirred for 15 minutes at 25-35° C
  3. customThe aqueous and organic layers were separated
  4. washthe organic layer was washed with brine
  5. washthe combined organic layers were washed with brine solution
  6. dry with materialThe organic layer was dried over Na2SO4
  7. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-613b8f625c524b7da8c537f18eaf0267
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08900625B2

反応ノート

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