Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007341Generated: October 28, 2026

P-Xylene → 7-Bromo-2-(3-fluoro-4-methoxyphenyl)-5-methoxy-1,3-benzoxazole

https://huagongshe.com/reaction/1007341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-XyleneHCID 7809—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-Bromo-6-[(3-fluoro-4-methoxybenzoyl)amino]-4-methoxyphenyl 3-fluoro-4-methoxybenzoateHCID 11179968—
SolventWaterHCID 962—
Product7-Bromo-2-(3-fluoro-4-methoxyphenyl)-5-methoxy-1,3-benzoxazoleHCID 1142810180.9%

Reaction Steps

A suspension of 2-bromo-6-[(3-fluoro-4-methoxybenzoyl)amino]-4-methoxyphenyl 3-fluoro-4-methoxybenzoate (46.0 g, 88.1 mmol), p-toluenesulfonic acid monohydrate (33.5 g, 177.2 mmol) and anhydrous p-xylene (1 l) was refluxed for 3 h with continuous water removal (Dean Stark Trap). The initial suspension turned into a brown solution at refluxing temperature. The solids were filtered off and washed with ethyl ether. The solids were suspended in ethyl ether (200 mL), stirred for 10 min, filtered off and dried to give a tan solid (25.1 g, m.p. 175-177° C.). The ethyl ether layer was concentrated to 20 mL and 2.5 g of additional product was obtained (90% overall yield). MS m/e 352 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794403B2
Source datasetuspto-grants-2004_09
ORD IDord-4953e42ae57c4717b2d17f5a7f4d7fbd
Source noteuspto-grants-2004_09