Ammonium Hydroxide → HCID 54704836, compound
Reaction equation
[C:1]([C:5]1[O:10][C:9](=O)[CH:8]=[C:7]([OH:12])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[NH4+:13].[OH-]>C1(C)C=CC=CC=1>[C:1]([C:5]1[NH:13][C:9](=[O:10])[CH:8]=[C:7]([OH:12])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 6-(tert-butyl)-4-hydroxy-2H-pyran-2-one (38 g, 168 mmol) and aq. NH4OH (150 mL, 30%) in dry toluene (200 mL) was heated at reflux for 1 h. The resulting mixture was concentrated and purified by CC (PE/EA=5/1) to give compound 17a (22.5 g, 80%) as a white solid.
Workup
- temperaturewas heated
- temperatureat reflux for 1 h
- concentrationThe resulting mixture was concentrated
- custompurified by CC (PE/EA=5/1)
Sources & evidence
- ORD record
- ord-3aa3da48cbfa4b77902b3f7462ee44d8
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946446B2
Reaction notes
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