Hydrochloric Acid → 2-(Hydroxymethyl)-4-methoxy-6-((2-nitrophenyl)diazenyl)phenol

HRID 1517759ノート

反応式

HRID 1517759 の反応式
[N+:1]([C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH2:6])([O-:3])=[O:2].Cl.[N:12]([O-])=O.[Na+].[OH-].[Na+].[OH:18][C:19]1[C:24](CO)=[CH:23][C:22]([O:27][CH3:28])=[CH:21][C:20]=1[CH2:29][OH:30].C1(O)C=CC=CC=1>O.S(=O)(=O)(O)N.C(O)C>[OH:30][CH2:29][C:20]1[CH:21]=[C:22]([O:27][CH3:28])[CH:23]=[C:24]([N:12]=[N:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[N+:1]([O-:3])=[O:2])[C:19]=1[OH:18]

参加物

10

反応物 6

HCID 313Hydrochloric Acid2 回HCID 996PhenolHCID 69462-NitroanilineHCID 14798Sodium Hydroxide2 回HCID 8274592,6-Bis(hydroxymethyl)-4-methoxyphenolHCID 23668193Sodium Nitrite

生成物 1

HCID 1363482922-(Hydroxymethyl)-4-methoxy-6-((2-nitrophenyl)diazenyl)phenol収率 55.8%

試薬・触媒・溶媒 3

HCID 5987Sulfamic Acid触媒HCID 702Ethanol溶媒2 回HCID 962Water溶媒5 回

反応条件

温度
0 °C

実験手順

In a 500 ml round bottom flask equipped with a magnetic stirrer was added 19.9 g (144 mmol) 2-nitroaniline (Aldrich), HCl(aq), 100 ml deionized water, and 100 ml EtOH. The mixture was cooled to 0° C. and 10.6 g (153 mmol) sodium nitrite in 50 ml water was added dropwise over 60 minutes while keeping the reaction mixture between −10-0° C. The reaction mixture was stirred for an additional 1 hour. 300 mg sulfamic acid was added to destroy excess nitrite and the mixture was stirred for an additional 20 minutes. The solids were filtered and the filtrate containing the diazonium salt was set aside and kept cold at −10° C. NaOH (29.3 g, 731 mmol) was dissolved in 100 ml water and approximately one-fourth was added to a solution of (2-hydroxy-5-methoxy-1,3-phenylene)dimethanol in 100 ml deionized water and 200 ml ethanol. The diazonium salt mixture and remaining sodium hydroxide solution were added to the reaction mixture containing the phenol derivative over a 1 hour period at 0° C. The reaction mixture was allowed to stir at 0° C. for 1 hour and ambient temperature for 3 hours. The contents were poured into 3 liters water and the pH was adjusted to 6 using 1N HCl. The resultant solid was washed with several liters of water and then dried at 55° C. for 40 hours using P2O5 as drying agent to afford 24.4 g (55.8%) of a dark solid which was used in the next step without further purification.

後処理

  1. customIn a 500 ml round bottom flask equipped with a magnetic stirrer
  2. custombetween −10-0° C
  3. customto destroy excess nitrite
  4. stirringthe mixture was stirred for an additional 20 minutes
  5. filtrationThe solids were filtered
  6. additionthe filtrate containing the diazonium salt
  7. customkept cold at −10° C
  8. additionwere added to the reaction mixture
  9. stirringto stir at 0° C. for 1 hour and ambient temperature for 3 hours
  10. washThe resultant solid was washed with several liters of water
  11. customdried at 55° C. for 40 hours
  12. customas drying agent

出典と根拠

ORDレコード
ord-671088327d54412db149942f417bb84e
出典データセット
uspto-grants-2012_07
特許番号
US08232326B2

反応ノート

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