Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872880Generated: November 1, 2026

HCID 10757175, compound → HCID 18687725, compound

https://huagongshe.com/reaction/1872880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10757175HCID 10757175—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventHydrogen BromideHCID 260—
ProductHCID 18687725HCID 1868772599.3%

Reaction Steps

A mixture of 3-fluoro-7-isopropoxyphenoxathiin 10,10-dioxide (Example 9) (3.51 g, 11.39 mmoles), tetrabutylammonium hydrogen sulfate (Aldrich) (0.654 g, 1.93 mmoles) and 48% aqueous hydrogen bromide (Acros) (80 mL) was refluxed with stirring for 45 minutes. The reaction was allowed to cool on an ice-bath, and the solid was collected, washed with water and dried in vacuo to give 3.010 g (99%) of 3-fluoro-7-hydroxyphenoxathiin 10,10-dioxide, mp 258-260° C. Recrystallization from ethyl acetate:hexanes gave the analytical sample, m.p. 250-260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06110961
Source datasetuspto-grants-2000_08
ORD IDord-ef965f9c495f4cd8be389c9044e066fc
Source noteuspto-grants-2000_08