Hydrochloric Acid → HCID 19070012, compound

HRID 2248947Notes

Reaction equation

HRID 2248947 reaction equation
[OH:1][C:2]1[CH:3]=[C:4](C(O)=O)[C:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:6][CH:7]=1.[OH-:17].[K+].[CH2:19](Br)[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].Cl.[CH2:35]([OH:37])C>O>[CH2:19]([O:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[CH:10][C:11]([C:35]([OH:37])=[O:17])=[CH:12][CH:13]=2)=[CH:4][CH:3]=1)[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]

Participants

7

Procedure

2.14 g of p-hydroxybiphenylcarboxylic acid and 1.12 g of potassium hydroxide were dissolved in a mixture of 300 ml of ethanol and 40 ml of water. Then 3.02 ml of tetradecyl bromide was added thereto and the mixture was heated under reflux for 12 hours. Next, 13.5 ml of 2M hydrochloric acid was added to the reaction mixture and the crystals thus precipitated were filtered. Thus 2.20 g of 4'-n-tetradecyloxybiphenyl-4-carboxylic acid was obtained.

Workup

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 12 hours
  3. customthe crystals thus precipitated
  4. filtrationwere filtered

Sources & evidence

ORD record
ord-b99fe1e8c9104f72850a7bae496a8e86
Source dataset
uspto-grants-1991_08
Patent number
US05041602

Reaction notes

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