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Water → 4-(6-Methyloctyloxy)benzoic acid

HRID 986097
ノート
印刷プレビュー

反応式

HRID 986097 の反応式
[OH-:1].[Na+].[OH2:3].Br[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH:10]([CH3:13])[CH2:11][CH3:12].[CH2:14]([OH:19])[CH2:15][CH2:16][CH2:17][CH3:18].CCO[CH2:23][CH3:24]>C(O)C>[CH3:13][CH:10]([CH2:11][CH3:12])[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][O:19][C:14]1[CH:24]=[CH:23][C:17]([C:18]([OH:3])=[O:1])=[CH:16][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 962WaterHCID 3283Diethyl EtherHCID 62761-PentanolHCID 14798Sodium HydroxideHCID 135481051-Bromo-6-methyloctane

生成物 1

HCID 134634574-(6-Methyloctyloxy)benzoic acid

試薬・触媒・溶媒 1

HCID 702
Ethanol
溶媒

実験手順

A 50-ml three-neck flask was charged with 2.01 g of sodium hydroxide, 10 ml of water and 20 ml of ethanol, and 3.16 g of 4-n-hydroxybenzoic acid was dissolved in the charge. 4.75 g of optically active 1-bromo-6-methyloctane synthesized from commercially available amyl alcohol was added to the mixture, and reaction was carried out for 19 hours under heat and reflux. After completion of the reaction, ether washing was conducted, and the aqueous layer was recovered by filtration and made acidic. The precipitated crystals were recovered by filtration and purified to obtain 4.75 g of 4-(6-methyloctyloxy)benzoic acid.

後処理

  1. dissolutionwas dissolved in the charge
  2. additionwas added to the mixture, and reaction
  3. temperatureunder heat
  4. temperaturereflux
  5. filtrationthe aqueous layer was recovered by filtration
  6. filtrationThe precipitated crystals were recovered by filtration
  7. custompurified

出典と根拠

ORDレコード
ord-9b060e2aaec645799eb9b3743018e24f
出典データセット
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04710585

反応ノート

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