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Dimethylformamide → 1-Bromo-5-isopropyl-2,4-bis-methoxymethoxy-benzene

HRID 1947173
ノート
印刷プレビュー

反応式

HRID 1947173 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[C:5]([OH:11])=[CH:4][C:3]=1[OH:12].CN(C)[CH:15]=[O:16].[CH2:18](N(C(C)C)C(C)C)C.[CH3:27][O:28][CH2:29]Cl>C(OCC)(=O)C>[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[C:5]([O:11][CH2:27][O:28][CH3:29])=[CH:4][C:3]=1[O:12][CH2:18][O:16][CH3:15]
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

6

反応物 4

HCID 6228DimethylformamideHCID 7864Chloromethyl Methyl EtherHCID 81531DiisopropylethylamineHCID 598299224-Bromo-6-(propan-2-YL)benzene-1,3-diol

生成物 1

HCID 598298701-Bromo-5-isopropyl-2,4-bis-methoxymethoxy-benzene収率 83.1%

試薬・触媒・溶媒 1

HCID 8857
Ethyl Acetate
溶媒

反応条件

温度
0 °C

実験手順

4-bromo-6-isopropyl-benzene-1,3-diol (IM1-a: 10.5 g, 45.5 mmol), dimethyl formamide (50 mL) and ethyldiisopropylamine (39.6 mL, 227 mmol) were placed in a 100 mL eggplant shaped flask, and the solution was cooled to 0° C., mixed with methoxymethylchloride (17.3 mL, 227 mmol) and the mixture was allowed to come to room temperature. After stirring for 12 hours the solution was heated to 50° C. and stirring was continued further for 6.5 hours. After completing the reaction, ethyl acetate was added, and after washing the organic layer 4 times with saturated sodium chloride, the organic layer was dried anhydrous sodium sulfate. After filtration and evaporation, the residue was purified by silica gel column chromatography to obtain the title compound (IM2-a: 12.1 g, 83.1%).

後処理

  1. customto come to room temperature
  2. temperaturewas heated to 50° C.
  3. stirringstirring
  4. waitwas continued further for 6.5 hours
  5. additionwas added
  6. washafter washing the organic layer 4 times with saturated sodium chloride
  7. filtrationAfter filtration and evaporation
  8. customthe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-0feda5b19cb3441c9966e115d8d35797
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399464B2

反応ノート

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