Trifluoroacetic acid → HCID 18990338, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]=1[OH:10])[CH2:5]O.FC(F)(F)C(O)=[O:17].[CH3:21][CH2:22][C:23](=[O:29])[C:24](=O)[CH2:25][CH2:26][CH3:27]>>[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:11]([O-:13])=[O:12])[C:9]=1[OH:10])[CH2:5][CH:24]([C:23](=[O:29])[CH2:22][CH3:21])[C:25](=[O:17])[CH2:26][CH3:27]Participants
4
Conditions
- Temperature
- 100 °C
Procedure
A mixture containing 0.2 g of 3,4-dihydroxy-5-nitrobenzyl alcohol and 0.03 ml of trifluoroacetic acid in 2.5 ml of 3,4-heptanedione was heated for 20 h at 100° C. The solvent was evaporated in vacuo and the residue was recrystallized from 2-propanol. Yield 0.3 g, mp 126°-131° C.
Workup
- customThe solvent was evaporated in vacuo
- customthe residue was recrystallized from 2-propanol
Sources & evidence
- ORD record
- ord-25e92bec5e6646baa2ab7a5488f9330f
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05489614
Reaction notes
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