Ethyl Acetoacetate → HCID 178472845、化合物

HRID 59624

反応式

HRID 59624 の反応式
Cl.[Br:2][C:3]1[C:4]([O:10][CH3:11])=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6].[N:12]([O-])=O.[Na+].[CH2:16]([O:18][C:19](=[O:24])[CH2:20][C:21]([CH3:23])=[O:22])[CH3:17].C(=O)(O)[O-].[Na+]>Cl.CO>[Br:2][C:3]1[C:4]([O:10][CH3:11])=[C:5]([NH:6][N:12]=[C:20]([C:21](=[O:22])[CH3:23])[C:19]([O:18][CH2:16][CH3:17])=[O:24])[CH:7]=[CH:8][CH:9]=1

参加物

7

反応物 4

HCID 8868Ethyl AcetoacetateHCID 516892Sodium BicarbonateHCID 23668193Sodium NitriteHCID 868104143-Bromo-2-Methoxyaniline hydrochloride

生成物 1

HCID 178472845HCID 178472845、化合物

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 887Methanol溶媒

実験手順

To a solution of 3-bromo-2-methoxyaniline hydrochloride (10 g) prepared as in Example 15, in hydrochloric acid (13.5 mL of concentrated hydrochloric acid in 136.5 mL of water) was added a solution of sodium nitrite (3.47 g in 10 mL of water) at about −5° C. to about 5° C. under stirring. The reaction mixture was stirred for about 1 hour at about −5° C. to about 5° C. Then ethylacetoacetate (6.55 g) was added to the reaction mixture and stirred for about 3 hours at about −5° C. to about 5° C. Sodium bicarbonate and methanol was then added to the reaction mixture. The reaction mixture was stirred at about −5° C. to about 5° C. for about 1 hour. The mixture was filtered to give a solid, which was washed with water and dried at about 50° C. to about 55° C. Yield: 13.3 g

後処理

  1. stirringThe reaction mixture was stirred for about 1 hour at about −5° C. to about 5° C
  2. stirringstirred for about 3 hours at about −5° C. to about 5° C
  3. stirringThe reaction mixture was stirred at about −5° C. to about 5° C. for about 1 hour
  4. filtrationThe mixture was filtered
  5. customto give a solid, which
  6. washwas washed with water
  7. customdried at about 50° C. to about 55° C

出典と根拠

ORDレコード
ord-e250670b322b43899edd2e2071c6b71d
出典データセット
uspto-grants-2016_09
特許番号
US09440927B2

関連ノート

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