Lithium Hydroxide → 2-(2,3,4-Trifluoroanilino)propionic acid

HRID 8442

反応式

HRID 8442 の反応式
[F:1][C:2]1[C:14]([F:15])=[C:13]([F:16])[CH:12]=[CH:11][C:3]=1[NH:4][CH:5]([CH3:10])[C:6]([O:8]C)=[O:7].[OH-].[Li+]>CO>[F:1][C:2]1[C:14]([F:15])=[C:13]([F:16])[CH:12]=[CH:11][C:3]=1[NH:4][CH:5]([CH3:10])[C:6]([OH:8])=[O:7]

参加物

4

反応物 2

HCID 3939Lithium HydroxideHCID 22015876Methyl2-(2,3,4-trifluoroanilino)propionate

生成物 1

HCID 220158662-(2,3,4-Trifluoroanilino)propionic acid収率 99.7%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Methyl 2-(2,3,4-trifluoroanilino)propionate (46.64 g) was dissolved in methanol (130 ml) and an aqueous solution (3 mol/l; 100 ml) of lithium hydroxide was slowly added thereto at 0° C. After stirring at room temperature for 3 hours, the solvent was evaporated. After adding water, the residue was washed with chloroform. Next, hydrochloric acid (6 mol/l) was slowly added to the aqueous layer until pH value reached 1. Then the aqueous layer was extracted with diisopropyl ether (IPE). The organic layer was dried over anhydrous magnesium sulfate and then the solvent was evaporated to give the title compound (43.7 g) as colorless crystals.

後処理

  1. customat 0° C
  2. customthe solvent was evaporated
  3. additionAfter adding water
  4. washthe residue was washed with chloroform
  5. additionNext, hydrochloric acid (6 mol/l) was slowly added to the aqueous layer until pH value
  6. extractionThen the aqueous layer was extracted with diisopropyl ether (IPE)
  7. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  8. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-8b10cb0936e1470cb7743fcc2219590f
出典データセット
uspto-grants-2006_08
特許番号
US07087778B2

関連ノート

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