Malic Acid → O-{4-[15-(Trifluoromethyl)pentadecylamino]benzoyl}malic acid

HRID 2058761Notes

Reaction equation

HRID 2058761 reaction equation
C([N:11]([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][C:36]([F:39])([F:38])[F:37])[C:12]1[CH:20]=[CH:19][C:15]([C:16](Cl)=[O:17])=[CH:14][CH:13]=1)(OCC1C=CC=CC=1)=O.C(N(CC)CC)C.[C:47]([OH:55])(=[O:54])[CH:48]([CH2:50][C:51]([OH:53])=[O:52])[OH:49].[H][H]>O1CCCC1.[Pd].CCOCC>[F:37][C:36]([F:38])([F:39])[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][NH:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([O:54][C:47](=[O:55])[CH:48]([CH2:50][C:51]([OH:53])=[O:52])[OH:49])=[O:17])=[CH:14][CH:13]=1

Participants

8

Procedure

A warm solution of 4-[N-carbobenzyloxy-15-(trifluoromethyl)pentadecylamino]benzoyl chloride and 1.3 g. triethylamine in 100 ml. ether is treated with 2 g. malic acid. An immediate precipitate forms, but the mixture is refluxed for one hour and filtered while hot. The solid is washed several times with hot ether, then the ether is evaporated to yield a white solid. The product is dissolved in tetrahydrofuran (100 ml.) and hydrogenated over 600 mg. 10% palladium-on-carbon at 50 psi until hydrogen uptake stops. The catalyst is filtered, and the solution is evaporated. The residue is crystallized from acetic acid to yield the product as a white solid.

Workup

  1. temperatureAn immediate precipitate forms, but the mixture is refluxed for one hour
  2. filtrationfiltered while hot
  3. washThe solid is washed several times with hot ether
  4. customthe ether is evaporated
  5. customto yield a white solid
  6. filtrationThe catalyst is filtered
  7. customthe solution is evaporated
  8. customThe residue is crystallized from acetic acid

Sources & evidence

ORD record
ord-99a46501b5cd4e2cb0c63d34f8bd4294
Source dataset
uspto-grants-1982_03
Patent number
US04318914

Reaction notes

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