Hydrochloric Acid → Benzenediazonium, 2-nitro-, chloride (1:1)

HRID 1447102

反応式

HRID 1447102 の反応式
[OH-].[Na+].CC(C1C=C(C(C)(C)C2C=CC=CC=2)C=CC=1O)(C)C1C=CC=CC=1.[N+:28]([C:31]1[CH:37]=[CH:36][CH:35]=[CH:34][C:32]=1[NH2:33])([O-:30])=[O:29].[ClH:38].[N:39]([O-])=O.[Na+]>CO.O.C(O)(=O)C>[Cl-:38].[N+:28]([C:31]1[CH:37]=[CH:36][CH:35]=[CH:34][C:32]=1[N+:33]#[N:39])([O-:30])=[O:29]

参加物

9

反応物 5

HCID 313Hydrochloric AcidHCID 69462-NitroanilineHCID 14798Sodium HydroxideHCID 760132,4-DicumylphenolHCID 23668193Sodium Nitrite

生成物 1

HCID 148932Benzenediazonium, 2-nitro-, chloride (1:1)

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒HCID 887Methanol溶媒2 回HCID 962Water溶媒2 回

反応条件

温度
2 °C

実験手順

Using the general procedure of Example 4, 13.6 grams (0.34 mole) of sodium hydroxide pellets were dissolved in 145 ml of methanol followed by the addition of 16.5 grams (0.05 mole) of 2,4-di-(α,α-dimethylbenzyl)phenol and an additional 20 ml of methanol. The resulting solution was cooled to 2° C. Meanwhile a solution of o-nitrobenzenediazonium chloride was prepared by diazotizing a mixture of 8.3 grams (0.06 mole) of o-nitroaniline and 17.3 grams of concentrated hydrochloric acid and 6 ml of water with a solution of 4.3 grams of sodium nitrite in 8 ml of water. The diazonium solution was added gradually to the alkaline solution over a two-hour period at 2° C. The resulting deep purple reaction mixture was stirred for 30 minutes at 2° C., and then acidified with 20 ml of glacial acetic acid.

出典と根拠

ORDレコード
ord-991ecd37ab57498a868edbdfaea3783f
出典データセット
uspto-grants-1982_02
特許番号
US04315848

関連ノート

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