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Hydrochloric Acid → 3-Chloro-4-(dodecyloxy)benzoic acid

HRID 1650647
ノート
印刷プレビュー

反応式

HRID 1650647 の反応式
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[Cl:11].[OH-].[Na+].[CH2:14](Br)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH3:25].Cl>CO.O1CCCC1.O>[CH2:25]([O:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[Cl:11])[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 313Hydrochloric AcidHCID 89191-BromododecaneHCID 14798Sodium Hydroxide2 回HCID 198603-Chloro-4-hydroxybenzoic acid

生成物 1

HCID 197391753-Chloro-4-(dodecyloxy)benzoic acid

試薬・触媒・溶媒 3

HCID 887Methanol溶媒
HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

In a mixed solvent of methanol and tetrahydrofuran was dissolved 5.17 g of 4-hydroxy-3-chlorobenzoic acid, and a solution of 2.4 g of sodium hydroxide in 5 ml of water was added to the solution. Then, 10 ml of n-dodecyl bromide was added dropwise to the mixture and the resulting mixture was refluxed for 2 hours. Then, 1.2 g of sodium hydroxide was further added and the mixture was refluxed for 1 hour. The thus-obtained solution was put in a 1N aqueous solution of hydrochloric acid, and the precipitate was recovered and filtration, washed with water and then with n-hexane and recrystallized from ethyl acetate to obtain 4.1 g of 4-n-dodecyloxy-3-chlorobenzoic acid.

後処理

  1. temperaturethe resulting mixture was refluxed for 2 hours
  2. temperaturethe mixture was refluxed for 1 hour
  3. customthe precipitate was recovered
  4. filtrationfiltration
  5. washwashed with water
  6. customwith n-hexane and recrystallized from ethyl acetate

出典と根拠

ORDレコード
ord-c202068f9f654ce5906e378d2f21177f
出典データセット
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04925591

反応ノート

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