4-(Octyloxy)benzoic acid → 4-Octyloxy-3-bromobenzoic acid

HRID 46414

反応式

HRID 46414 の反応式
[CH2:1]([O:9][C:10]1[CH:18]=[CH:17][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[Br:19]Br>O>[CH2:1]([O:9][C:10]1[CH:11]=[CH:12][C:13]([C:14]([OH:16])=[O:15])=[CH:17][C:18]=1[Br:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

参加物

4

反応物 2

HCID 172314-(Octyloxy)benzoic acidHCID 24408Bromine

生成物 1

HCID 233334474-Octyloxy-3-bromobenzoic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A 25 g (0.1 mole) amount of p-octyloxybenzoic acid was suspended in 120 ml of water. The temperature was increased to between 50° C. and 55° C. and 17.6 g (0.11 mole) of bromine were added over a period of 7 hours at that temperature. The suspended solids were then filtered and recrystallized from ethanol and pure 4-octyloxy-3-bromobenzoic acid was obtained.

後処理

  1. temperatureThe temperature was increased to between 50° C. and 55° C.
  2. filtrationThe suspended solids were then filtered
  3. customrecrystallized from ethanol

出典と根拠

ORDレコード
ord-a3cd020d4ab04b65b1bc5990ffdfda26
出典データセット
uspto-grants-1979_11
特許番号
US04173545

関連ノート

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