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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965609Generated: October 31, 2026

Boron tribromide → HCID 22312839, compound

https://huagongshe.com/reaction/965609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 11369272HCID 11369272—
SolventDichloromethaneHCID 6344—
ProductHCID 22312839HCID 2231283975%

Reaction Steps

A solution of 7-(4-methoxyphenoxy)-2H-1,4-benzoxazin-3(4H)-one (120 mg; 0.44 mmol) in CH2Cl2 (1 ml) was treated with BBr3 (332 mg; 1.33 mmol). The mixture was stirred at room temperature for 3 hours. After evaporation to dryness the residue was taken up in EtOAc and water. The organic phase was washed with brine and dried over MgSO4. The residue (110 mg) was triturated with EtOAc, filtered and dried to give 7-(4-hydroxyphenoxy)-2H-1,4-benzoxazin-3(4H)-one as a biege solid (85 mg), Melting point 250-251° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951855B2
Source datasetuspto-grants-2005_10
ORD IDord-3e206261e7004635aa66b5d8b102812a
Source noteuspto-grants-2005_10