Sulfuric Acid → 2,2,2-Trifluoroethyl 3-hydroxybenzoate

HRID 2220028ノート

反応式

HRID 2220028 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[F:11][C:12]([F:16])([F:15])[CH2:13]O.S(=O)(=O)(O)O>>[OH:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([O:7][CH2:13][C:12]([F:16])([F:15])[F:11])=[O:6]

参加物

4

反応条件

温度
95 °C

実験手順

Into a 250 mL round bottom flask equipped with magnetic stirrer and heating mantle was added 10 parts of 3-hydroxy benzoic acid, 100 parts of 2,2,2-trifluoroethanol and 0.5 parts of concentrated sulfuric acid. The reaction mixture was heated at 95° C. for 48 hours. The solvent was evaporated under reduced pressure and the solid material was dissolved in 250 mL of ethyl acetate. The organic layer was washed with 250 mL of water, 250 mL 5% solution of sodium bicarbonate in 100 mL of water and finally with 250 mL of water. The ethyl acetate layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure, yield 4.1 parts. TLC on silica gel plate showed a single spot. The structure was confirmed on the basis of 1H NMR. The reaction proceeded as follows:

後処理

  1. customInto a 250 mL round bottom flask equipped with magnetic stirrer
  2. temperatureheating mantle
  3. customThe solvent was evaporated under reduced pressure
  4. dissolutionthe solid material was dissolved in 250 mL of ethyl acetate
  5. washThe organic layer was washed with 250 mL of water, 250 mL 5% solution of sodium bicarbonate in 100 mL of water and finally with 250 mL of water
  6. dry with materialThe ethyl acetate layer was dried over anhydrous sodium sulfate
  7. customthe solvent was evaporated under reduced pressure
  8. customyield 4.1 parts

出典と根拠

ORDレコード
ord-487b98d3afcd4dc4b9c3f925d79a992a
出典データセット
uspto-grants-2008_08
特許番号
US07416898B2

反応ノート

読み込み中…