Ammonium formate → 4-Methoxy-2-(propan-2-yl)phenol

HRID 81779

反応式

HRID 81779 の反応式
O[C:2]([C:5]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:6]=1[OH:13])([CH3:4])[CH3:3].C([O-])=O.[NH4+]>CC(O)=O.O.[Pd]>[CH:2]([C:5]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:6]=1[OH:13])([CH3:4])[CH3:3]

参加物

6

反応物 2

HCID 2723923Ammonium formateHCID 252417532-(2-Hydroxypropan-2-YL)-4-methoxyphenol

生成物 1

HCID 183649974-Methoxy-2-(propan-2-yl)phenol収率 97%

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

To a solution of 2-(1-hydroxy-1-methyl-ethyl)-4-methoxy-phenol (50.57 g, 278 mmol) in 550 ml AcOH was added 10% Pd/C (as a slurry in 20 ml H2O) Ammonium formate (87.52 g, 1388 mmol) was added in portions. The mixture was warmed to 100° C. for 1 hour, cooled and filtered through a pad of celite. The celite pad was washed with ethyl acetate. The mother liquor was mixed with H2O and extracted with ethyl acetate. The combined organics were washed with H2O, washed with brine, dried over Na2SO4, filtered and concentrated in vacuo to give 2-isopropyl-4-methoxy-phenol (44.74 g, 97%) as a pale yellow oil.

後処理

  1. additionwas added in portions
  2. temperaturecooled
  3. filtrationfiltered through a pad of celite
  4. washThe celite pad was washed with ethyl acetate
  5. additionThe mother liquor was mixed with H2O
  6. extractionextracted with ethyl acetate
  7. washThe combined organics were washed with H2O
  8. washwashed with brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ae4b24557d6b49009a4414d37c4a6811
出典データセット
uspto-grants-2014_09
特許番号
US08846705B2

関連ノート

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