2-Furancarbonyl chloride → HCID 68122418, compound

HRID 328438Notes

Reaction equation

HRID 328438 reaction equation
[CH3:1][N:2]([CH2:26][CH2:27][OH:28])[C:3](=[O:25])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]/[CH:15]=[CH:16]\[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24].[O:29]1[CH:33]=[CH:32][CH:31]=[C:30]1[C:34](Cl)=[O:35]>>[CH3:1][N:2]([CH2:26][CH2:27][O:28][C:34]([C:30]1[O:29][CH:33]=[CH:32][CH:31]=1)=[O:35])[C:3](=[O:25])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14]/[CH:15]=[CH:16]\[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24]

Participants

3

Reactant 2

HCID 682422-Furancarbonyl chlorideHCID 86734640HCID 86734640, compound

Product 1

HCID 68122418HCID 68122418, compound

Procedure

N-methyl-N-(2-furoyloxyethyl)erucamide was prepared by the procedure of example 1 from 39.5 gms. (0.1 mole) of N-methyl-N-(2-hydroxyethyl)erucamide 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)erucamide was prepared by the procedure of example 1 from 39.5 gms

Sources & evidence

ORD record
ord-82a71b26daf64f3a8c6e9bf2a3c03c1f
Source dataset
uspto-grants-1977_04
Patent number
US04017522

Reaction notes

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