Pyridine → Tetradecanoic Acid 1-(2-hex-3-enyloxycarbonyl-ethyl)-heptyl Ester

HRID 2304958Notes

Reaction equation

HRID 2304958 reaction equation
[CH2:1]([O:7][C:8](=[O:19])[CH2:9][CH2:10][CH:11]([OH:18])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[CH2:2][CH:3]=[CH:4][CH2:5][CH3:6].N1C=CC=CC=1.CN(C1C=CC=CN=1)C.[C:35](Cl)(=[O:49])[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH3:48]>O1CCCC1.O>[CH2:1]([O:7][C:8]([CH2:9][CH2:10][CH:11]([O:18][C:35](=[O:49])[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH3:48])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])=[O:19])[CH2:2][CH:3]=[CH:4][CH2:5][CH3:6]

Participants

7

Reactant 4

HCID 1049PyridineHCID 218852-DimethylaminopyridineHCID 66986Myristoyl chlorideHCID 542574244-Hydroxy-decanoic acid hex-3-enyl ester

Product 1

HCID 53781700Tetradecanoic Acid 1-(2-hex-3-enyloxycarbonyl-ethyl)-heptyl EsterYield 92.5%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8028TetrahydrofuranSolvent2×

Procedure

To a mixture of 1.10 g of 4-hydroxy-decanoic acid hex-3-enyl ester, 0.64 g pyridine and 0.1 g dimethylaminopyridine in 5 ml tetrahydrofuran was slowly added a solution of 1.10 g myristoyl chloride in 5 ml tetrahydrofuran. The mixture was stirred for 16 hours at room temperature. Water was then added and the mixture extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate, 2N hydrochloric acid, water, dried over magnesium sulfate and evaporated to dryness. The residue was chromatographed on silica gel to give 1.81 g of a colorless liquid.

Workup

  1. extractionthe mixture extracted with ethyl acetate
  2. washThe organic layer was washed with saturated sodium bicarbonate, 2N hydrochloric acid, water
  3. dry with materialdried over magnesium sulfate
  4. customevaporated to dryness
  5. customThe residue was chromatographed on silica gel

Sources & evidence

ORD record
ord-cfd3a55a941f4de3bd2da2af4d10e533
Source dataset
uspto-grants-2002_08
Patent number
US06437150B1

Reaction notes

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