Hydrochloric Acid → 4-(4-Methoxybenzyl)cyclohexanecarboxylic acid

HRID 262206

反応式

HRID 262206 の反応式
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][C:6]([CH2:7][C:8]2[CH:16]=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[CH:10][CH:9]=2)=[CH:5][CH:4]=1.[Na].Cl.C1(C(O)=O)CCCCC=1>C(O)CC(C)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][CH:8]2[CH2:9][CH2:10][CH:11]([C:12]([OH:14])=[O:13])[CH2:15][CH2:16]2)=[CH:17][CH:18]=1

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 694701-Cyclohexene-1-carboxylic acidHCID 2579874-(4-Methoxybenzyl)benzoic acidHCID 5360545Sodium

生成物 1

HCID 124638444-(4-Methoxybenzyl)cyclohexanecarboxylic acid

試薬・触媒・溶媒 1

HCID 31260Isoamyl Alcohol溶媒

実験手順

A solution of 49.5 g. of 4-(4-methoxybenzyl)benzoic acid (Example 1c) in 1000 ml. of isoamyl alcohol was heated at reflux and 109 g. of sodium was added in pieces over a 40 minute period. The reaction mixture was heated under reflux for three hours, then cooled and steam distilled until 2.5 liters of distillate was obtained. The resulting aqueous solution was acidified with concentrated hydrochloric acid and extracted with ether. The ether extracts were dried over anhydrous magnesium sulfate and the solvent removed to give 34 g. of a crystalline residue comprising a mixture of the desired compound with the corresponding cyclohex-1-enecarboxylic acid. The latter mixture was dissolved in 170 ml. of ethanol and hydrogenated in the presence of 3 g. of 10% palladium-on-carbon catalyst. The catalyst was filtered off and the solvent removed to give 34 g. of 4-(4-methoxybenzyl)cyclohexanecarboxylic acid, used directly in the next reaction without further purification.

後処理

  1. temperatureat reflux
  2. temperatureThe reaction mixture was heated
  3. temperatureunder reflux for three hours
  4. temperaturecooled
  5. distillationsteam distilled until 2.5 liters of distillate
  6. customwas obtained
  7. extractionextracted with ether
  8. dry with materialThe ether extracts were dried over anhydrous magnesium sulfate
  9. customthe solvent removed
  10. customto give 34 g

出典と根拠

ORDレコード
ord-d825497ddc644ca18bbbb67c5831e7d9
出典データセット
uspto-grants-1979_05
特許番号
US04153719

関連ノート

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