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

HRID 1277581

반응식

HRID 1277581 반응식
[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]

참가 물질

9

반응물 5

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

생성물 1

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

시약·촉매·용매 3

HCID 176Acetic Acid용매HCID 887Methanol용매2회HCID 962Water용매2회

반응 조건

온도
2 °C

실험 절차

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.

출처 및 근거

ORD 기록
ord-1e64be9eede44b998135a75d1d5dfede
출처 데이터셋
uspto-grants-1981_07
특허 번호
US04278589

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