2-Aminomethyl-4-tert-butyl-6-iodophenol hydrochloride → 5-tert-Butyl-2-hydroxy-3-(methylthio)benzaldehyde

HRID 236921

反応式

HRID 236921 の反応式
Cl.NCC1C=C(C(C)(C)C)C=C(I)C=1[OH:15].Cl.N[CH2:18][C:19]1[CH:24]=[C:23]([C:25]([CH3:28])([CH3:27])[CH3:26])[CH:22]=[C:21]([S:29][CH3:30])[C:20]=1[OH:31]>>[CH3:30][S:29][C:21]1[CH:22]=[C:23]([C:25]([CH3:28])([CH3:27])[CH3:26])[CH:24]=[C:19]([CH:18]=[O:15])[C:20]=1[OH:31]

参加物

3

反応物 2

HCID 126342632-Aminomethyl-4-tert-butyl-6-iodophenol hydrochlorideHCID 213146452-Aminomethyl-4-(1,1-dimethylethyl)-6-(methylthio)phenol hydrochloride

生成物 1

HCID 130974015-tert-Butyl-2-hydroxy-3-(methylthio)benzaldehyde

実験手順

This compound is prepared essentially by the same procedure as described in Example 3, Step A, except that the 2-aminomethyl-4-(1,1-dimethylethyl)-6-iodophenol hydrochloride is replaced by 2-aminomethyl-4-(1,1-dimethylethyl)-6-(methylthio)phenol hydrochloride. Thereby is obtained 3-methylthio-5-(1,1-dimethylethyl)salicylaldehyde.

後処理

  1. customThis compound is prepared essentially by the same procedure

出典と根拠

ORDレコード
ord-ee3c2c4ac748432e932e27d080819bf0
出典データセット
uspto-grants-1979_06
特許番号
US04159279

関連ノート

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