Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Propanol | HCID 1031 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 20064236 | HCID 20064236 | — |
| Product | HCID 19437279 | HCID 19437279 | 90% |
Reaction Steps
59.7 g allyl chloride were added dropwise at 95° C. to a solution of 87.9 g of 2,6-bis-(3-hydroxyphenoxy)-pyridine (prepared according to DE-A 19 34 889 from 2,6-dichloropyridine and 2 moles of resorcinol; colorless crystals of melting point 188° C.) and 26.4 g of sodium hydroxide in 500 ml of n-propanol. The mixture was refluxed for a further 10 hours and then cooled to room temperature, after which 500 ml of dichloromethane were added and the precipitated sodium chloride was filtered off. After the solvent had been distilled off under reduced pressure, 101 g (90%) of product were obtained as a yellowish oil having a viscosity of 60 mPa.s at 50° C.; NMR (300 MHZ, D6-DMSO): 4.56 (d, 4H, allyl), 5.22-5.42 (dd, 4H, allyl), 5.95-6.10 (m, 2H, allyl), 6.60-6.85 (m, 6H, arom.), 7.22 (t, 2H, arom.), 7.82 (t, 1H, arom.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05003017 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-453c69d240e74373ac13e357512e921d |
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| Source note | uspto-grants-1991_03 |
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