4-Tert-octylphenol → 4-Tert-octylcatechol

HRID 1605631ノート

反応式

HRID 1605631 の反応式
N1C(C[OH:8])=CC=CC=1CO.[C:11]([C:19]1[CH:24]=[CH:23][C:22]([OH:25])=[CH:21][CH:20]=1)([CH2:14][C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:13])[CH3:12]>>[C:11]([C:19]1[CH:24]=[C:23]([OH:8])[C:22](=[CH:21][CH:20]=1)[OH:25])([CH2:14][C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:12])[CH3:13]

参加物

3

反応物 2

HCID 88144-Tert-octylphenolHCID 709572,6-Pyridinedimethanol

生成物 1

HCID 708284-Tert-octylcatechol収率 54%

実験手順

The procedure of Example 9 was repeated, except 0.2% by weight of pyridine-2,6-dimethanol was used as a catalyst and the reaction was carried out at 50°C. Consequently, the conversion of para-tert.-octyl phenol was 6.2%, 4-tert.-octyl pyrocatechol was formed in a yield of 54% based on the converted octyl phenol and the conversion of perpropionic acid was 97.2%.

後処理

  1. customwas carried out at 50°C

出典と根拠

ORDレコード
ord-ddd0ec0ccbb34c49886d92e5782d39dc
出典データセット
uspto-grants-1976_04
特許番号
US03950437

反応ノート

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