Cetyl Alcohol → HCID 14419825, compound

HRID 1582853Notes

Reaction equation

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

Participants

Reactant 2

HCID 2682Cetyl Alcohol

HCID 74323,5-Dinitrobenzoyl chloride

Product 1

HCID 14419825HCID 14419825, compoundYield 90%

Procedure

Using 3,5-dinitrobenzoyl chloride (60.6 g, 263.0 mmol) and hexadecyl alcohol (63.9 g, 263.9 mmol), n-hexadecyl-3,5-dinitrobenzoate was obtained (103.2 g, yield: 90%) in the same manner as in Example 1.

Sources & evidence

ORD record: ord-a8e2ae435af642069c6240e91ec5e389
Source dataset: uspto-grants-2004_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06740371B1

Reaction notes

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