Ethanol → 3,3,3-Trifluoro-2-(trifluoromethyl)-1-(hydroxymethyl)propylamine

HRID 1594286ノート

反応式

HRID 1594286 の反応式
[F:1][C:2]([F:14])([F:13])[CH:3]([C:9]([F:12])([F:11])[F:10])[CH:4]([C:6](O)=[O:7])[NH2:5].B.C1COCC1.CCOC(C)=O.CCO>C1COCC1.O>[F:1][C:2]([F:13])([F:14])[CH:3]([C:9]([F:10])([F:11])[F:12])[CH:4]([NH2:5])[CH2:6][OH:7]

参加物

7

反応条件

温度
25 °C

実験手順

A solution of 4,4,4,4′,4′,4′-hexafluoro-DL-valine (0.500 g, 2.22 mmol) in THF (20 mL) was stirred under nitrogen at 25° C. Borane-THF complex (6.66 mL, 1.0 M in THF) was added dropwise and the resulting solution stirred for 4 h at 25° C. After this time period, the reaction was complete by TLC (10:2:1 EtOAc:EtOH:H2O). The reaction mixture was quenched by slow addition of 10% HOAc in MeOH (23 mL). After concentration, the residue was dissolved in Et2O (200 mL) and washed with saturated aqueous NaHCO3 (3×20 mL) and brine (20 mL), and then dried using Na2SO4. After concentration, the resulting residue was used directly in the next reaction without further purification.

後処理

  1. customThe reaction mixture was quenched by slow addition of 10% HOAc in MeOH (23 mL)
  2. concentrationAfter concentration
  3. dissolutionthe residue was dissolved in Et2O (200 mL)
  4. washwashed with saturated aqueous NaHCO3 (3×20 mL) and brine (20 mL)
  5. customdried
  6. concentrationAfter concentration
  7. customthe resulting residue was used directly in the next reaction without further purification

出典と根拠

ORDレコード
ord-bd5fa1ac19e647339eae81a8b406f37b
出典データセット
uspto-grants-2007_11
特許番号
US07300951B2

反応ノート

読み込み中…