HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Chloro-4,6-bis(4-methoxyphenyl)-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178491912 | HCID 178491912 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Chloro-4,6-bis(4-methoxyphenyl)-1,3,5-triazine | HCID 19086184 | — |
Reaction Steps
A Grignard solution of p-methoxyphenylmagnesium bromide (prepared from 12.2 g (0.05 mol) of magnesium and 93.5 g (0.5 mol) of p-bromoanisole in 130 ml of anhydrous THF) is added to a solution of 31.3 g (0.17 mol) of cyanuric chloride in 100 ml of THF over a period of 1.5 hours while maintaining the temperature in the range from 0° to 20° C. After addition is complete, the mixture is stirred at room temperature for 1.5 hours and then poured into 150 ml of 12% hydrogen chloride solution in an ice-bath. The beige suspension is filtered off, washed neutral with water and then washed with methanol. The crude product is recrystallized from 350 ml of toluene to give the compound of the formula ##STR21##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05591850 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-ebf64fc2288843c88f7a6308cbb70e4c |
| Source note | uspto-grants-1997_01 |