HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 86743097, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chlororesorcinol | HCID 1731 | — |
| Reactant | 2,6-Dimethylol-p-cresol | HCID 7039 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | HCID 86743097 | HCID 86743097 | — |
Reaction Steps
2,6-Bis(hydroxymethyl)-p-cresol (25 g, 0.149 moles), 4-chlororesorcinol (18.26 g, 0.126 moles and p-toluenesulfonic acid monohydrate (0.67 g, 0.0035 moles) were heated for 5.5 hours at 65°-70° C. in 37 mL 2-ethoxyethanol. The reaction mixture was diluted with 125 mL 2-ethoxyethanol and added dropwise to 1.5 L rapidly stirring H2O. The solid was collected by filtration, reslurried in 1 L H2O and refiltered. This process was repeated twice and the solid vacuum dried to yield 38.49 g. See Tables 1 and 2 for glass transition and alkaline dissolution data. The ortho-, ortho-linkages of the alternating copolymers and the terminal groups were identified by 13C NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04970287 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-2b238d2395e04905b1adc4d1607f308b |
| Source note | uspto-grants-1990_11 |