Lauric Acid → HCID 18996052, compound

HRID 374864Notes

Reaction equation

HRID 374864 reaction equation
[CH3:1][C:2]1([CH3:11])[O:7][CH2:6][C:5]([NH2:10])([CH2:8][CH3:9])[CH2:4][O:3]1.[C:12](O)(=[O:24])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].C1CCC(N=C=NC2CCCCC2)CC1.ON1C2C=CC=CC=2N=N1>C(Cl)Cl>[CH3:11][C:2]1([CH3:1])[O:3][CH2:4][C:5]([NH:10][C:12](=[O:24])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])([CH2:8][CH3:9])[CH2:6][O:7]1

Participants

6

Reactant 4

HCID 3893Lauric AcidHCID 10868DicyclohexylcarbodiimideHCID 757711-HydroxybenzotriazoleHCID 134044275-Ethyl-2,2-dimethyl-1,3-dioxan-5-amine

Product 1

HCID 18996052HCID 18996052, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

2,2-Dimethyl-5-amino-5-ethyl-1,3-dioxane is acylated wih dodecanoic acid in methylene chloride in the presence of DCC and 1-hydroxybenzo-triazole. Filtration and concentration gives the product.

Workup

  1. filtrationFiltration and concentration
  2. customgives the product

Sources & evidence

ORD record
ord-97db55875b46461f8dc390904839ed60
Source dataset
uspto-grants-1996_01
Patent number
US05482965

Reaction notes

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