HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-bromo-3-trifluoromethyl-5-methoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine-N-oxide | HCID 12151305 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-bromo-3-trifluoromethyl-5-methoxypyridine | HCID 23503604 | 49.1% |
Reaction Steps
Using 7.2 g (18 mmol) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine-N-oxide, 7 ml of toluene, 17 ml of dimethylformamide and 10 g (35 mmol) of phosphorus oxybromide, 4.1 g (yield 49%) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-2-bromo-3-trifluoromethyl-5-methoxypyridine (compound No. 124; m.p. 145-147° C.) was obtained in the same process as in Synthesis Example 9 step (f).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06770662B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-594cda97293a452996ccf596eaa16bb5 |
| Source note | uspto-grants-2004_08 |