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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003342Generated: November 1, 2026

Nitrogen → 7-Bromo-3-chloro-6-methoxy-1,2-benzisoxazole

https://huagongshe.com/reaction/1003342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantBromineHCID 24408—
Reactant3-Chloro-6-methoxy-1,2-benzoxazoleHCID 15816924—
ReactantCCl4 acetoneHCID 19595110—
SolventAcetic AcidHCID 176—
Product7-Bromo-3-chloro-6-methoxy-1,2-benzisoxazoleHCID 18796450—

Reaction Steps

To a stirred solution of 3-chloro-6-methoxy-1,2-benzisoxazole (25 g) in acetic acid (200 ml) was added a solution of bromine (32.6 g) in acetic acid (100 ml) dropwise under N2 at ambient temperature. The mixture was allowed to stir overnight. TLC (silica gel, 5% acetone/CCl4) revealed the presence of starting material. Additional bromine (11 g) in acetic acid (50 ml) was added, and the reaction mixture was allowed to stir overnight. The reaction was filtered and washed with water. The precipitate was collected and recrystallized from methanol to yield the desired compound, m.p. 134-135° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046203
Source datasetuspto-grants-2000_04
ORD IDord-9a5d4d24130f478a888b2aab9dcbf1b0
Source noteuspto-grants-2000_04