Potassium Carbonate → 1-((4-Bromo-2,5-dichlorophenoxy)methyl)adamantane

HRID 1427891

反応式

HRID 1427891 の反応式
[Br:1][C:2]1[C:7]([Cl:8])=[CH:6][C:5]([OH:9])=[C:4]([Cl:10])[CH:3]=1.CS(O[CH2:16][C:17]12[CH2:26][CH:21]3[CH2:22][CH:23]([CH2:25][CH:19]([CH2:20]3)[CH2:18]1)[CH2:24]2)(=O)=O.C(=O)([O-])[O-].[K+].[K+]>O>[Br:1][C:2]1[C:7]([Cl:8])=[CH:6][C:5]([O:9][CH2:16][C:17]23[CH2:26][CH:21]4[CH2:20][CH:19]([CH2:25][CH:23]([CH2:22]4)[CH2:24]2)[CH2:18]3)=[C:4]([Cl:10])[CH:3]=1

参加物

5

反応条件

温度
125 °C

実験手順

A mixture of 4-bromo-2,5-dichlorophenol (1.35 g, 5.58 mmol), adamantan-1-ylmethyl methanesulfonate (Fr. Demande, 2909090, 30 May 2008) (1.5 g, 6.14 mmol), and potassium carbonate (0.85 g, 6.14 mmol) in N,N-dilmethylformamide (10 mL) was stirred at 65° C. for 16 h and at 125° C. for 48 h. The reaction mixture was cooled down to ambient temperature, diluted with water (40 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine (50 mL), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography eluting with a 5% to 10% gradient of ethyl acetate in hexanes to afford 1-((4-bromo-2,5-dichlorophenoxy)methyl)adamantine as a colorless solid (1.7 g, 71%): MS (ES+) m/z 391.3 (M+1);

後処理

  1. temperatureThe reaction mixture was cooled down to ambient temperature
  2. extractionextracted with ethyl acetate (2×50 mL)
  3. washThe combined organic layers were washed with brine (50 mL)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by column chromatography
  8. washeluting with a 5% to 10% gradient of ethyl acetate in hexanes
  9. customto afford 1-((4-bromo-2,5-dichlorophenoxy)methyl)adamantine as a colorless solid (1.7 g, 71%)

出典と根拠

ORDレコード
ord-2d4ca2c844d5491b812dc7bc6ffe5c34
出典データセット
uspto-grants-2015_01
特許番号
US08933236B2

関連ノート

読み込み中…