Ethanol → 4-(Tetradecyloxy)benzoic acid

HRID 483558

反応式

HRID 483558 の反応式
[CH2:1]([O:15][C:16]1[CH:25]=[CH:24][C:19]([C:20]([O:22]C)=[O:21])=[CH:18][CH:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[OH-].[K+].CO.C(O)C>O>[CH2:1]([O:15][C:16]1[CH:17]=[CH:18][C:19]([C:20]([OH:22])=[O:21])=[CH:24][CH:25]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]

参加物

6

反応物 4

HCID 702EthanolHCID 887MethanolHCID 14797Potassium HydroxideHCID 3312490Methyl 4-(tetradecyloxy)benzoate

生成物 1

HCID 2894104-(Tetradecyloxy)benzoic acid収率 90.3%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 120 g of methyl p-(tetradecyloxy)benzoate, 57.96 g of potassium hydroxide, 1-liter of methyl alcohol, 400 ml of ethyl alcohol and 60 ml of water is refluxed for 4.5 hours. A solid is formed and the reaction mixture partitioned between dilute hydrochloric acid and chloroform with some warming. The organic layer is washed with warm dilute hydrochloric acid and dried. The filtrate is evaporated to a volume of 600 ml and an equal volume of hexanes added to form a solid which is dried to give 104 g of the desired product as a white solid, m.p. 94°-96° C.

後処理

  1. temperatureis refluxed for 4.5 hours
  2. customA solid is formed
  3. customthe reaction mixture partitioned between dilute hydrochloric acid and chloroform with some warming
  4. washThe organic layer is washed
  5. temperaturewith warm dilute hydrochloric acid
  6. customdried
  7. customThe filtrate is evaporated to a volume of 600 ml
  8. additionan equal volume of hexanes added
  9. customto form a solid which
  10. customis dried

出典と根拠

ORDレコード
ord-e0ccab45b2da47f5aaab0822f3be4f1c
出典データセット
uspto-grants-1993_07
特許番号
US05225425

関連ノート

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