Guaiacol → HCID 18008626, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[OH:9].[CH3:10][CH2:11][CH2:12][CH2:13][CH:14]([CH:16]([CH3:18])C)C.[CH3:19][CH2:20]CC(CC(C)C)C.CC(CC(C(C)C)C)C>>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH2:19][CH2:20][CH2:18][CH2:16][CH2:14][CH2:13][CH2:12][CH2:11][CH3:10])[CH:6]=[CH:5][C:4]=1[OH:9]Participants
3
Reactant 2
Product 1
Conditions
- Temperature
- 120 °C
Procedure
2-Methoxyphenol (5 mol, 621 g), dry Amberlyst 15 (50 g) and tripropylene (5.5 mol, 694 g, 951 ml) were placed in a 3000 ml 3N RBF. The mixture was heated and maintained at 120° C. under vigorous stirring for 7 hrs. After cooling to ambient temperature, the reaction mixture was filtered and distilled to obtain 2-methoxy-4-nonylphenol in vacuo.
Workup
- temperatureThe mixture was heated
- temperatureAfter cooling to ambient temperature
- filtrationthe reaction mixture was filtered
- distillationdistilled
Sources & evidence
- ORD record
- ord-8926835667504e3ca3f10a57c80d3118
- Source dataset
- uspto-grants-2003_10
- Patent number
- US06632410B2
Reaction notes
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