Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Propanol | HCID 1031 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | HCID 22475984 | HCID 22475984 | — |
| Solvent | M-Xylene | HCID 7929 | — |
| Product | HCID 178458112 | HCID 178458112 | — |
Reaction Steps
A 500 mL round-bottomed flask fitted with a condenser, a magnetic stirrer and a nitrogen atmosphere is charged with 5.48 g (0.0169 mol) of 4,6-bis-(2,4-dimethylphenyl-2-chloro-s-triazine, 10.2 g (0.169 mol) of n-propanol, 2,37 g (0.0246 mol) of methane-sulfonic acid and 25 mL of m-xylene. The mixture is stirred at 90° C. for one hour. The mixture is then allowed to cool to room temperature and vacuum filtered through a plug of silica gel which is subsequently washed with 95:5 heptane:ethyl acetate. The combined organic layers are vacuum filtered through another plug of silica gel. The solvent is removed under reduced pressure to afford 3.31 g of the title compound as off-white crystals melting at 86-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06242598B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-c2ddea4917cf451984bf5e47bdd93558 |
|---|
| Source note | uspto-grants-2001_06 |
|---|