Pyridine → 2-(2',6'-Diisopropylphenylazo)-4,6-ditertbutylphenol

HRID 10606

反応式

[CH:1]([C:4]1[CH:10]=[CH:9][CH:8]=[C:7]([CH:11]([CH3:13])[CH3:12])[C:5]=1[NH2:6])([CH3:3])[CH3:2].C1([O-])C=CC=CC=1.[C:21]([C:25]1[CH:30]=[C:29]([C:31]([CH3:34])([CH3:33])[CH3:32])[CH:28]=[CH:27][C:26]=1[OH:35])([CH3:24])([CH3:23])[CH3:22].[OH-].[Na+].[N:38]1C=CC=CC=1>C1(C)C=CC=CC=1.O>[CH:11]([C:7]1[CH:8]=[CH:9][CH:10]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:5]=1[N:6]=[N:38][C:27]1[CH:28]=[C:29]([C:31]([CH3:34])([CH3:33])[CH3:32])[CH:30]=[C:25]([C:21]([CH3:24])([CH3:23])[CH3:22])[C:26]=1[OH:35])([CH3:13])[CH3:12]

参加物

実験手順

This phenol was prepared, as described for above, from a theoretical yield of 7.4 mmol of diazotized 2,6-diisopropylaniline and a phenolate solution comprised of 2,4-Ditertbutylphenol (1.42 g), water (15 mL), NaOH (0.5 g), pyridine (3 mL), and toluene (6 mL) Yield=0.98 g (36%).

出典と根拠

ORDレコード: ord-327e3218e975482ebbe892dcbab483af
出典データセット: uspto-grants-2006_08
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US07094848B2

反応式

参加物

反応物 5

生成物 1

試薬・触媒・溶媒 2

実験手順

出典と根拠

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