Octadecyl isocyanate → HCID 19018987, compound

HRID 1757856Notes

Reaction equation

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

Participants

Reactant 2

HCID 66988Octadecyl isocyanate

HCID 35051094-Nitrocatechol

Product 1

HCID 19018987HCID 19018987, compound

Procedure

Using this procedure, the reaction of 4-nitrocatechol with octadecyl isocyanate gave 3,4-bis [[(octadecylamino)carbonyl]oxy]nitrobenzene (mp 117°-121°). The structure was confirmed by the nmr spectrum.

Sources & evidence

ORD record: ord-16ff1f7907b04e948a4c3ddc947b7ad2
Source dataset: uspto-grants-1995_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05446189

Reaction notes

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