P-Anisidine → 195314-31-9

HRID 1457592

반응식

HRID 1457592 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[CH:5][CH:4]=1.[N:10]([O-])=O.[Na+].[CH3:14][O:15][C:16]1[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([C:23]([CH3:26])([CH3:25])[CH3:24])[CH:17]=1.[OH-].[Na+]>Cl>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]=[N:10][C:20]2[CH:21]=[C:16]([O:15][CH3:14])[CH:17]=[C:18]([C:23]([CH3:26])([CH3:25])[CH3:24])[C:19]=2[OH:22])=[CH:5][CH:4]=1

참가 물질

6

반응물 4

HCID 7732P-AnisidineHCID 8456Butylated HydroxyanisoleHCID 14798Sodium HydroxideHCID 23668193Sodium Nitrite

생성물 1

HCID 135719544195314-31-9수율 64.4%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매2회

실험 절차

p-Anisidine (257 g) was dissolved in 514 ml of conc. hydrochloric acid, and under ice-cooling, 1530 ml of an aqueous solution containing 158 g of sodium nitrite was added dropwise to the solution. This mixture was added dropwise under ice-cooling to 3000 ml of an aqueous solution containing 356 g of 4-methoxy-2-tert-butylphenol and 416 g of sodium hydroxide. The resulting mixture was stirred at the same temperature for 15 minutes. Conc. hydrochloric acid (about 400 ml) was added dropwise to the reaction mixture to adjust pH of the mixture to 3, and the precipitated crystals were collected by filtration. The crystals were washed and dried, and recrystallized from a mixed solution of chloroform and ethanol to give 400 g of 2-(4-methoxyphenylazo)-4-methoxy-6-tert-butylphenol (yield: 64%, melting point: 125°-127° C., IR: 1600 cm-1).

후처리

  1. temperatureunder ice-cooling
  2. additionwas added dropwise to the solution
  3. additionThis mixture was added dropwise under ice-
  4. filtrationthe precipitated crystals were collected by filtration
  5. washThe crystals were washed
  6. customdried
  7. customrecrystallized from a mixed solution of chloroform and ethanol

출처 및 근거

ORD 기록
ord-b437a585c04944d18271f66039854825
출처 데이터셋
uspto-grants-1998_12
특허 번호
US05849732

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