Ethanol → HCID 23131628, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH:26]=[CH:27][C:28]=1[N+:29]([O-:31])=[O:30])[C:5]([C:7]1[CH:12]=[CH:11][C:10]([O:13]C(=O)C2C=CC([N+]([O-])=O)=C(C)C=2)=[CH:9][CH:8]=1)=[O:6].C(O)C.[OH-].[Na+]>O>[OH:13][C:10]1[CH:11]=[CH:12][C:7]([C:5]([C:4]2[CH:26]=[CH:27][C:28]([N+:29]([O-:31])=[O:30])=[C:2]([CH3:1])[CH:3]=2)=[O:6])=[CH:8][CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
322 g (1 mol) of 4-nitro-4′-(4-nitrobenzoyloxy)benzophenone (example 4.1) are heated in 1.3 l of water, 200 ml of ethanol and 85 g of sodium hydroxide until the solid has dissolved.
Sources & evidence
- ORD record
- ord-007c13379ad14ef4b6df5baf1dae91ee
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409859B2
Reaction notes
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