Diethylene Glycol → HCID 86743027, compound
Reaction equation
[CH2:1]([OH:7])[CH2:2][O:3][CH2:4][CH2:5][OH:6].[N+:8]([C:11]1[CH:19]=[CH:18][C:14]([C:15](Cl)=[O:16])=[CH:13][CH:12]=1)([O-:10])=[O:9]>>[N+:8]([C:11]1[CH:19]=[CH:18][C:14]([C:15]([C:1]([OH:7])([C:15](=[O:16])[C:14]2[CH:13]=[CH:12][C:11]([N+:8]([O-:10])=[O:9])=[CH:19][CH:18]=2)[CH2:2][O:3][CH2:4][CH2:5][OH:6])=[O:16])=[CH:13][CH:12]=1)([O-:10])=[O:9]Participants
3
Procedure
Diethylene glycol (31.8 g, 0.3 mole) and p-nitrobenzoyl chloride (116 g, 0.62 mole) were reacted under the conditions described in Example 1, Part A. The product was crystallized from ethyl acetate to give bis-(4-nitrobenzoyl)-diethylene glycol (101 g) as a pale yellow solid, m.p. 100°-102° C. The product was homogeneous by TLC.
Workup
- customThe product was crystallized from ethyl acetate
Sources & evidence
- ORD record
- ord-94871ac009784dadb5313817ca971116
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04829099
Reaction notes
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