Nitric Acid → HCID 54176741, compound
Reaction equation
[N+:1]([O-:4])(O)=[O:2].[CH:5]1([C:11]2[CH:16]=[CH:15][C:14]([CH2:17][C:18]([OH:20])=[O:19])=[C:13]([OH:21])[CH:12]=2)[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1>C(Cl)Cl>[CH:5]1([C:11]2[C:16]([N+:1]([O-:4])=[O:2])=[CH:15][C:14]([CH2:17][C:18]([OH:20])=[O:19])=[C:13]([OH:21])[CH:12]=2)[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.06 ml of 100% nitric acid are slowly added dropwise at -10° to a solution of 5.9 g of 4-cyclohexyl-2-hydroxy-phenylacetic acid in 100 ml of absolute methylene chloride. The mixture is finally stirred for 10 minutes without further cooling, the methylene chloride solution washed several times with water, dried over sodium sulphate and evaporated to yield the title compound.
Workup
- washthe methylene chloride solution washed several times with water
- dry with materialdried over sodium sulphate
- customevaporated
Sources & evidence
- ORD record
- ord-0718a6c7756b4a7e9a03faafa529caac
- Source dataset
- uspto-grants-1981_02
- Patent number
- US04252817
Reaction notes
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