Formaldehyde → Formaldehyde;phenol
Reaction equation
[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C=O.[OH-].[Na+].C1(C)C=CC(S(O)(=O)=O)=CC=1.NC(N)=O>>[CH2:1]=[O:7].[C:1]1([OH:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
Conditions
- Temperature
- 80 °C
Procedure
Phenol ( 1 mol) and 50% formalin (0.6 mol) were charged to a reaction vessel and the temperature maintained below 40° C. whilst sodium hydroxide (0.004 mol) was added. The temperature was then raised to 80° C. The temperature was maintained at 80° C. while a second charge of 50% formalin (1.0 mol) was added slowly over 30 minutes and the temperature maintained at 80° C. for a further 15 minutes. The mixture was then held at 70° C. for a further 30 minutes. The pH was adjusted with p-toluene sulphonic acid solution to 4.0 +/-0.2 and the volatiles distilled off under vacuum at 70° C. to a viscosity of 80 centistokes at 25° C. The resin was cooled to 60° C., the pH adjusted to 6.2 +/-0.02 with sodium hydroxide, 0.027 moles of urea were added and the product further concentrated to a final viscosity of 500 cP at 25° C., cooled and discharged.
Workup
- additionwas added
- temperatureThe temperature was maintained at 80° C. while
- additionwas added slowly over 30 minutes
- temperaturethe temperature maintained at 80° C. for a further 15 minutes
- distillationthe volatiles distilled off under vacuum at 70° C. to a viscosity of 80 centistokes at 25° C
- temperatureThe resin was cooled to 60° C.
- additionwere added
- concentrationthe product further concentrated to a final viscosity of 500 cP at 25° C.
- temperaturecooled
Sources & evidence
- ORD record
- ord-492bec93932549deadc5497694d25ccc
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05051454
Reaction notes
Loading…