Hydrochloric Acid → alpha-Acetyl-alpha-[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenylazo]benzenepropanamide

HRID 263065ノート

反応式

HRID 263065 の反応式
[F:1][C:2]([F:17])([F:16])[C:3]([C:9]1[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][CH:10]=1)([OH:8])[C:4]([F:7])([F:6])[F:5].Cl.[N:19]([O-])=O.[Na+].C([O-])(=O)C.[Na+].[C:28]([CH:31]([CH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)[C:32]([NH2:34])=[O:33])(=[O:30])[CH3:29]>C(O)C.O>[C:28]([C:31]([N:19]=[N:15][C:12]1[CH:13]=[CH:14][C:9]([C:3]([OH:8])([C:4]([F:6])([F:5])[F:7])[C:2]([F:16])([F:17])[F:1])=[CH:10][CH:11]=1)([CH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)[C:32]([NH2:34])=[O:33])(=[O:30])[CH3:29]

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 517045Sodium AcetateHCID 5778012-(4-Aminophenyl)-1,1,1,3,3,3-hexafluoropropan-2-olHCID 27840922-Benzyl-3-oxobutanamideHCID 23668193Sodium Nitrite

生成物 1

HCID 21318133alpha-Acetyl-alpha-[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenylazo]benzenepropanamide

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A mixture of 10.4 g. (0.04 mol) of 4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)-ethyl]benzenamine and 36 ml. of 4 N hydrochloric acid was maintained at 2° or below while a solution of 2.76 g. (0.04 mol) of sodium nitrite in 10 ml. of water was added. The reaction was stirred for an additional 30 minutes in the ice bath, 12.0 g. of sodium acetate was added, followed by a slurry of 7.65 g. (0.04 mol) of α-acetylbenzenepropanamide in 50 ml. of ethanol. The cooling bath was removed; after 30 minutes, when the temperature was 6°, 50 ml. of methanol was added and the resulting solution was stirred an additional 80 minutes at ambient temperature. The reaction was diluted with water and extracted with dichloromethane. The extracts were dried over sodium sulfate, passed over a small amount of silica gel and concentrated under vacuum to give 19.28 g. of crude α-acetyl-α-[4-[2,2,2 -trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenylazo]benzenepropanamide as an orange oil which gradually crystallized. This material was recrystallized only with difficulty and was generally used as is for subsequent reactions. An analytical sample was prepared by repeated solution in dichloromethane, dilution with tetrachloromethane and slow evaporation of the dichloromethane to give α-acetyl-α-[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenylazo]benzenepropanamide as yellow crystals, m.p. 128°-133°.

後処理

  1. additionA mixture of 10.4 g
  2. customThe cooling bath was removed
  3. customwas 6°
  4. additionof methanol was added
  5. additionThe reaction was diluted with water
  6. extractionextracted with dichloromethane
  7. dry with materialThe extracts were dried over sodium sulfate
  8. concentrationconcentrated under vacuum
  9. customto give 19.28 g
  10. customof crude α-acetyl-α-[4-[2,2,2 -trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenylazo]benzenepropanamide as an orange oil which gradually crystallized
  11. customThis material was recrystallized only with difficulty
  12. customAn analytical sample was prepared by repeated solution in dichloromethane
  13. customdilution with tetrachloromethane and slow evaporation of the dichloromethane

出典と根拠

ORDレコード
ord-6628d5c2df6b4497992899125b908ecc
出典データセット
uspto-grants-1979_05
特許番号
US04156016

反応ノート

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