Dodecanamide, N-(3-hydroxypropyl)- → HCID 19893767, compound

HRID 892909Notes

Reaction equation

HRID 892909 reaction equation
[OH:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:18])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[CH3:19][C:20]1([CH3:36])[O:25][CH:24]([C:26]([NH:28][CH2:29][CH2:30][C:31](O)=[O:32])=[O:27])[C:23]([CH3:35])([CH3:34])[CH2:22][O:21]1>>[CH3:19][C:20]1([CH3:36])[O:25][CH:24]([C:26]([NH:28][CH2:29][CH2:30][C:31]([O:1][CH2:2][CH2:3][CH2:4][NH:5][C:6](=[O:18])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])=[O:32])=[O:27])[C:23]([CH3:35])([CH3:34])[CH2:22][O:21]1

Participants

3

Reactant 2

HCID 9903248Dodecanamide, N-(3-hydroxypropyl)-HCID 189385173-[N-(2,2,5,5-Tetramethyl-1,3-dioxane-4-carbonyl)amino]propionic acid

Product 1

HCID 19893767HCID 19893767, compoundYield 64.1%

Procedure

N-(3-Hydroxypropyl)dodecanamide (2.57 g) and 2.59 g of 3-[N-(2,2,5,5-tetramethyl-1,3-dioxane-4-carbonyl)amino]propionic acid were reacted in the same manner as in Example 15 to obtain 3.19 g of the title compound (yield: 64%)

Sources & evidence

ORD record
ord-7e39deca5df449c3ac9d0f716e6ecacd
Source dataset
uspto-grants-1992_06
Patent number
US05120738

Reaction notes

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