Octanoic Acid → HCID 131731985, compound

HRID 540990Notes

Reaction equation

HRID 540990 reaction equation
[CH2:1]([OH:6])[CH:2]([OH:5])[CH2:3][OH:4].[CH2:7]([OH:12])[CH:8]([OH:11])[CH2:9][OH:10].[CH2:13]([OH:18])[CH:14]([OH:17])[CH2:15][OH:16].[CH2:19]([OH:24])[CH:20]([OH:23])[CH2:21][OH:22].[C:25](O)(=O)[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].CCN=C=NCCCN(C)C.Cl>C1COCC1>[CH2:25]([CH:2]([CH2:1][CH2:7][CH2:8][CH3:9])[C:3]([OH:4])=[O:16])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].[OH:24][CH2:19][CH:20]([CH2:21][OH:22])[OH:23].[OH:18][CH2:13][CH:14]([CH2:15][OH:16])[OH:17].[OH:12][CH2:7][CH:8]([CH2:9][OH:10])[OH:11].[OH:6][CH2:1][CH:2]([CH2:3][OH:4])[OH:5]

Participants

5

Reactant 3

HCID 379Octanoic AcidHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 1970823756491-53-3

Product 1

HCID 131731985HCID 131731985, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Into a 250 mL vessel, tetraglycerol (5.0 g, 15.91 mmol) was added and dissolved into anhydrous THF (50 mL). Octanoic acid (15.12 mL, 95.44 mmol) was also dissolved into the reaction mixture which was stirred magnetically at room temperature for one hour to fully dissolve the reagents. N,N-dimethylaminopyridine (0.194 g, 1.59 mmol) was dissolved in the solution. When the catalyst was fully dissolved, EDC HCl (18.32 g, 95.6 mmol) was added into the vessel and was sealed to keep the reaction dry. The reaction proceeded overnight at 55° C. The solution was stripped of THF via rotoevaporation and redissolved into chloroform. The organic layer was washed 2× with sodium bicarbonate buffer and 2× with deionized water to remove unreacted starting materials. The chloroform was removed to yield a clear viscous liquid. NMR analysis supported full conversion of hydroxyl groups to the octanoic esters.

Workup

  1. dissolutionto fully dissolve the reagents
  2. dissolutionWhen the catalyst was fully dissolved
  3. customwas sealed
  4. customdry
  5. waitThe reaction proceeded overnight at 55° C
  6. dissolutionredissolved into chloroform
  7. washThe organic layer was washed 2× with sodium bicarbonate buffer and 2× with deionized water
  8. customto remove unreacted
  9. customThe chloroform was removed
  10. customto yield a clear viscous liquid

Sources & evidence

ORD record
ord-cb5862b86c6f4c6ab8875b249374fa8e
Source dataset
uspto-grants-2014_10
Patent number
US08871819B2

Reaction notes

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