Sulfuric Acid → 4-Phenyl-2-nitrobenzenediazonium hydrogen sulfate

HRID 48564

反応式

HRID 48564 の反応式
[S:1](=[O:5])(=[O:4])([OH:3])[OH:2].[N:6]([O-])=O.[Na+].[N+:10]([C:13]1[CH:14]=[C:15]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:16]=[CH:17][C:18]=1[NH2:19])([O-:12])=[O:11].C(OCC)C>C(O)(=O)C>[S:1]([O-:5])([OH:4])(=[O:3])=[O:2].[C:20]1([C:15]2[CH:16]=[CH:17][C:18]([N+:19]#[N:6])=[C:13]([N+:10]([O-:12])=[O:11])[CH:14]=2)[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

参加物

6

反応物 4

HCID 1118Sulfuric AcidHCID 3283Diethyl EtherHCID 77705[1,1'-Biphenyl]-4-amine, 3-nitro-2 回HCID 23668193Sodium Nitrite2 回

生成物 1

HCID 858226914-Phenyl-2-nitrobenzenediazonium hydrogen sulfate

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
20 °C

実験手順

To 70 mL of sulfuric acid at 10° C. is added portionwise sodium nitrite (7 g, 0.1 mol). The reaction mixture is warmed to 20° C. to dissolve all the sodium nitrite and then cooled to 15° C. To the reaction mixture is added over 30 minutes a suspension of 3-nitro-4-amino-1,1′-biphenyl (7.33 g, 0.034 mol), prepared in (B) above, in 60 mL of acetic acid. The reaction mixture is stirred for one hour at 10° C. and then to the reaction mixture is added 500 mL of diethyl ether. An exotherm occurs. The mixture is stirred for one hour. The solid formed is removed by filtration behind a safety shield and washed with diethyl ether to give 16.2 g of the title compound as a yellow solid. The solid is dried for 1.5 hours at 20° C. under vacuum and stored in a freezer in a polyethylene container until later use. Analysis: IR (nujol) v 1650 (N═N), 2250 (N2+) cm−1.

後処理

  1. temperaturecooled to 15° C
  2. additionTo the reaction mixture is added over 30 minutes
  3. stirringThe mixture is stirred for one hour
  4. customThe solid formed
  5. customis removed by filtration behind a safety shield
  6. washwashed with diethyl ether

出典と根拠

ORDレコード
ord-b81197e5af114fd2834c650810480dc0
出典データセット
uspto-grants-2004_03
特許番号
US06703510B2

関連ノート

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