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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858234Generated: November 1, 2026

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

https://huagongshe.com/reaction/858234

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 11428101—

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 numberUS07148247B2
Source datasetuspto-grants-2006_12
ORD IDord-a6f7f789a7da40c0adcbb748cfc45d50
Source noteuspto-grants-2006_12