2-Furancarbonyl chloride → HCID 54217028, compound

HRID 328432Notes

Reaction equation

HRID 328432 reaction equation
[CH3:1][N:2]([CH2:16][CH2:17][OH:18])[C:3](=[O:15])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[O:19]1[CH:23]=[CH:22][CH:21]=[C:20]1[C:24](Cl)=[O:25]>>[CH3:1][N:2]([CH2:16][CH2:17][O:18][C:24]([C:20]1[O:19][CH:23]=[CH:22][CH:21]=1)=[O:25])[C:3](=[O:15])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]

Participants

3

Reactant 2

HCID 682422-Furancarbonyl chlorideHCID 11737000Dodecanamide, N-(2-hydroxyethyl)-N-methyl-

Product 1

HCID 54217028HCID 54217028, compound

Procedure

N-methyl-N-(2-furoyloxyethyl)lauramide was prepared by the procedure of example 1 from 26 gms. (0.1 mole) of N-methyl-N-(2-hydroxyethyl)lauramide and 13 gms. (0.1 mole) of furoyl chloride. The structure of the final product was characterized on the basis of IR and NMR spectral analyses as described in example 1.

Workup

  1. customN-methyl-N-(2-furoyloxyethyl)lauramide was prepared by the procedure of example 1 from 26 gms

Sources & evidence

ORD record
ord-47c9343cd7a84b2bbf3f0a362a8460e2
Source dataset
uspto-grants-1977_04
Patent number
US04017522

Reaction notes

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