1-Bromooctadecane → 3-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester

HRID 488256Notes

Reaction equation

HRID 488256 reaction equation
[C:1]1([CH2:7][O:8][C:9](=[O:18])[C:10]2[CH:15]=[C:14]([OH:16])[CH:13]=[C:12]([OH:17])[CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.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][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O.CN(C=O)C>[C:1]1([CH2:7][O:8][C:9](=[O:18])[C:10]2[CH:11]=[C:12]([O:17][CH2:37][CH2:36][CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH3:20])[CH:13]=[C:14]([OH:16])[CH:15]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

6

Reactant 3

HCID 82181-BromooctadecaneHCID 11430Potassium CarbonateHCID 11299537HCID 11299537, compound

Product 1

HCID 152334763-Hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl esterYield 36%

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 6228DimethylformamideSolvent

Procedure

A mixture of 30 g (0.123 mol) of 3,5-dihydroxybenzoic acid phenylmethyl ester, 40.9 g (0.123 mol) of 1-bromooctadecane, 17 g (0.123 mol) of anhydrous potassium carbonate in 500 ml of acetone and 10 ml of DMF was stirred at reflux for 25 hours. The reaction mixture was filtered and the filtrate was concentrated at reduced pressure to a solid. The residue was treated with water and the product was extracted with methylene chloride. The dried extract was concentrated at reduced pressure to a solid which was purified by HPLC using 1% ethyl acetate-methylene chloride to give 22 g (36% yield, mp 72°-75°) of 3-hydroxy-5-(octadecyloxy)benzoic acid phenylmethyl ester. The structure was confirmed by nmr and mass spectra.

Workup

  1. temperatureat reflux for 25 hours
  2. filtrationThe reaction mixture was filtered
  3. concentrationthe filtrate was concentrated at reduced pressure to a solid
  4. additionThe residue was treated with water
  5. extractionthe product was extracted with methylene chloride
  6. extractionThe dried extract
  7. concentrationwas concentrated at reduced pressure to a solid which
  8. customwas purified by HPLC

Sources & evidence

ORD record
ord-ab294117e5ce4f7cbb10f82e43eb63d4
Source dataset
uspto-grants-1994_03
Patent number
US05298652

Reaction notes

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