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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835421Generated: October 31, 2026

Toluene → 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-bromo-3-trifluoromethyl-5-methoxypyridine

https://huagongshe.com/reaction/1835421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosphorus oxybromideHCID 24613—
Reactant4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine-N-oxideHCID 12151305—
SolventDimethylformamideHCID 6228—
Product4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-bromo-3-trifluoromethyl-5-methoxypyridineHCID 2350360449.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770662B2
Source datasetuspto-grants-2004_08
ORD IDord-594cda97293a452996ccf596eaa16bb5
Source noteuspto-grants-2004_08