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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937741Generated: October 31, 2026

Water → HCID 9886735, compound

https://huagongshe.com/reaction/1937741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
ReactantBis(trifluoroacetoxy)iodobenzeneHCID 102317—
ReactantTidembersatHCID 170378—
SolventAcetonitrileHCID 6342—
ProductHCID 9886735HCID 988673536%

Reaction Steps

(3R,4S)-6-Acetyl-4-(3,5-difluorobenzamido)-3,4-dihydro-2,2-dimethyl-3-hydroxy-2H-1-benzopyran D3 (1.88 g, 5.0 mmol) (Example 4 of WO95/34545) was dissolved in acetonitrile (25ml), water (5 ml) and trifluoroacetic acid (0.77 ml, 10.0 mmol). [Bis(trifluoroacetoxy)iodo]benzene (4.30 g, 10.0 mmol) was added and the reaction stirred under reflux for three hours. The reaction mixture was allowed to cool and the acetonitrile was removed in vacuo, the resulting material being partitioned between water (50 ml) and dichloromethane (125 ml). The aqueous layer was extracted with further portions of dichloromethane (3×25 ml) and the combined organic extracts were dried over magnesium sulphate, filtered and the solvent removed in vacuo. The resulting yellow solid was purified by column chromatography on silica, eluting with 20% to 40% ethyl acetate in hexane to afford the title compound as a white solid (0.70 g, 36%, m.p. 179.4° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395909B1
Source datasetuspto-grants-2002_05
ORD IDord-735a55d5d83d4290a4e1b986af91af95
Source noteuspto-grants-2002_05