1,2-Dichlorobenzene → HCID 19736319、化合物

HRID 257295

反応式

HRID 257295 の反応式
C(O[C:12]1[CH:13]=[C:14]2[C:19](=[CH:20][CH:21]=1)[CH:18]=[C:17]([C:22]([NH:24][C:25]1[CH:30]=[C:29]([CH2:31][CH2:32][CH2:33][CH3:34])[CH:28]=[CH:27][C:26]=1[OH:35])=O)[CH:16]=[CH:15]2)CCCCCCCCC.[OH2:36].[C:37]1([CH3:47])[CH:42]=[CH:41][C:40](S(O)(=O)=O)=[CH:39][CH:38]=1.Cl[C:49]1[CH:54]=CC=C[C:50]=1Cl>>[CH2:50]([O:36][C:12]1[CH:13]=[C:14]2[C:19](=[CH:20][CH:21]=1)[CH:18]=[C:17]([C:22]1[O:35][C:26]3[CH:27]=[CH:28][C:29]([CH2:31][CH2:32][CH2:33][CH3:34])=[CH:30][C:25]=3[N:24]=1)[CH:16]=[CH:15]2)[CH2:49][CH2:54][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:37][CH3:47]

参加物

4

反応物 3

HCID 72391,2-Dichlorobenzene2 回HCID 521998p-Toluenesulfonic acid monohydrateHCID 197363202-(6-Decyloxy-2-naphthoylamino)-4-butylphenol

生成物 1

HCID 19736319HCID 19736319、化合物収率 61.3%

実験手順

In a 20 ml-round-bottomed flask, 0.95 g (2.00 mM) of 2-(6-decyloxy-2-naphthoylamino)-4-butylphenol, 0.07 g of p-toluenesulfonic acid monohydrate and 8 ml of o-dichlorobenzene were placed, followed by stirring for 30 min. at 200°-203° C. After the reaction, o-dichlorobenzene was distilled-off under reduced pressure. The residue was purified by silica gel column chromatography (eluent: toluene/hexane=1/1) and recrystallized from acetone) to obtain 0.56 g of 2-(6-decyloxy-2-naphthyl)-5-butyl-benzoxazole (yield: 61.3%). ##STR28##

後処理

  1. customThe residue was purified by silica gel column chromatography (eluent: toluene/hexane=1/1)
  2. customrecrystallized from acetone)

出典と根拠

ORDレコード
ord-7df6945a2ca34b739f4d2271c69d809c
出典データセット
uspto-grants-1993_11
特許番号
US05262083

関連ノート

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