Hydrochloric Acid → HCID 14329788, compound

HRID 1606929Notes

Reaction equation

HRID 1606929 reaction equation
[CH2:1](/[C:3](=[CH:9]\[CH3:10])/[CH:4]=[CH:5]/[C:6]([OH:8])=O)[CH3:2].ON1C(=O)CCC1=O.C1(N=C=NC2CCCCC2)CCCCC1.[NH2:34][CH2:35][C:36]([OH:38])=[O:37].Cl>O1CCOCC1.O1CCCC1.O.C(N(CC)CC)C>[CH2:1](/[C:3](=[CH:9]\[CH3:10])/[CH:4]=[CH:5]/[C:6]([NH:34][CH2:35][C:36]([OH:38])=[O:37])=[O:8])[CH3:2]

Participants

10

Procedure

To a solution of (E,E)-4-ethyl-2,4-hexadienoic acid (2.8 g) and N-hydroxysuccinimide (2.3 g) in dioxane (20 ml) was added dicyclohexylcarbodiimide (4.32 g). The mixture was stirred at ambient temperature overnight and then filtered. The filtrate was concentrated to dryness under reduced pressure to give a residue which was dissolved in tetrahydrofuran (100 ml). To the solution was added a solution of glycine (4.5 g) and triethylamine (8.34 ml) in water (60 ml). The resulting mixture was stirred at ambient temperature for 5 hours, acidified with 1N hydrochloric acid and then extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate, and then concentrated to dryness under reduced pressure to give a crystalline residue. The residue was triturated with a mixture of chloroform and hexane to give N-[(E,E)-4-ethyl-2,4-hexadienoyl]glycine (1.72 g).

Workup

  1. filtrationfiltered
  2. concentrationThe filtrate was concentrated to dryness under reduced pressure
  3. customto give a residue which
  4. stirringThe resulting mixture was stirred at ambient temperature for 5 hours
  5. extractionextracted with ethyl acetate
  6. washThe extract was washed with water
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated to dryness under reduced pressure
  9. customto give a crystalline residue
  10. customThe residue was triturated with a mixture of chloroform and hexane

Sources & evidence

ORD record
ord-61175da0c6584dd18e403cf562b9bdfb
Source dataset
uspto-grants-1989_09
Patent number
US04863926

Reaction notes

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