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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445951Generated: October 31, 2026

Bromine → HCID 57567188, compound

https://huagongshe.com/reaction/1445951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantHCID 13987268HCID 13987268—
SolventAcetonitrileHCID 6342—
ProductHCID 57567188HCID 575671886%

Reaction Steps

A stirred solution of 5-{hydroxy-[2-(trifluoromethyl)phenyl]methyl}-4-methoxy-5H-furan-2-one (2.9 g, 10.1 mmol) in acetonitrile at room temperature is treated dropwise with bromine (0.52 ml, 10.1 mmol), stirred for 24 h and concentrated in vacuo. The resultant residue is diluted with CH2Cl2 and triethylamine (4.25 ml), cooled in an ice bath, treated with methane sulfonyl chloride (1.6 ml), stirred for 0.5 h at ice bath temperatures, allowed to warm to room temperature for 2 h and diluted with EtOAc and water. The organic phase is separated, dried over MgSO4 and concentrated in vacuo. This residue is flash chromatographed (SiO2, hexane/EtOAc as eluent) to afford the title product as a white solid, 0.20 g (6% yield), mp 136-138° C., identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666904B2
Source datasetuspto-grants-2010_02
ORD IDord-d9356142d7464b668e231a10daf08b1e
Source noteuspto-grants-2010_02