Hydrochloric Acid → 4'-Decyloxybiphenyl-4-carboxylic Acid

HRID 1417

반응식

HRID 1417 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([OH:16])=[O:15])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[CH2:17](Br)[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26].[OH-].[K+].[I-].[Na+].Cl>O.C(O)C>[CH2:17]([O:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([OH:16])=[O:15])=[CH:10][CH:9]=2)=[CH:6][CH:7]=1)[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]

참가 물질

8

반응 조건

온도
100 °C

실험 절차

A mixture of 21.4 g (0.1 mol) of 4'-hydroxybiphenyl-4-carboxylic acid, 33.15 g (0.15 mol) of n-decyl bromide, 13.20 g (0.2 mol) of 85% potassium hydroxide, 1.05 g (7 mmol) of sodium iodide, 500 ml of ethanol and 100 ml of distilled water was heated under reflux at 100° C. for 12 hours. After 40 ml of 25% potassium hydroxide was added, the mixture was further heated under reflux for 2 hours. After allowing the reaction system to cool up to room temperature, the reaction mixture in cold water was acidified with 36% hydrochloric acid. The deposited product was separated by filtration and dissolved in acetone with heating, followed by filtration. The resulting filtrate was concentrated to obtain 1.97 g (6 mmol) of 4'-decyloxybiphenyl-4-carboxylic acid.

후처리

  1. temperaturewas heated
  2. temperaturethe mixture was further heated
  3. temperatureunder reflux for 2 hours
  4. temperatureto cool up to room temperature
  5. customThe deposited product was separated by filtration
  6. dissolutiondissolved in acetone
  7. temperaturewith heating
  8. filtrationfollowed by filtration
  9. concentrationThe resulting filtrate was concentrated

출처 및 근거

ORD 기록
ord-0396fca3395e4ebeb8f2c15f2dea83c8
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05725798

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