Hydroquinone → HCID 87127190, compound
Reaction equation
[CH3:1][C:2]1[C:3]([N:11]=[C:12]=[O:13])=[CH:4][C:5]([N:8]=[C:9]=[O:10])=[CH:6][CH:7]=1.[C:14]([O:19][CH2:20][CH2:21][OH:22])(=[O:18])[C:15]([CH3:17])=[CH2:16].C1(C=CC(O)=CC=1)O>>[CH3:1][C:2]1[C:3]([N:11]=[C:12]=[O:13])=[CH:4][C:5]([N:8]=[C:9]=[O:10])=[CH:6][CH:7]=1.[C:14]([O:19][CH2:20][CH2:21][OH:22])(=[O:18])[C:15]([CH3:17])=[CH2:16]Participants
4
Conditions
- Temperature
- 80 °C
Procedure
A one litter, three-neck flask was charged with 348 parts of tolylene diisocyanate (TDI) and heated to 80° C. Then, 260 parts of 2-hydroxyethyl methacrylate (2-HEMA), 0.07 part of tin octylate, and 0.05 part of hydroquinone were dripped while temperature was controlled to 80° C. After dripping, the sample was stirred at 80° C. for 3 hours and taken out. Thus, TDI-2-HEMA adduct was obtained.
Workup
- customwas controlled to 80° C
Sources & evidence
- ORD record
- ord-0df397ec8c9a42feb8a9b34386a0e419
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07026371B2
Reaction notes
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