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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716322Generated: November 3, 2026

4-Methoxyphenol → 3-[4-(4-Methoxy-phenoxy)-benzenesulfonyl]-1-trityloxy-azepan-2-one

https://huagongshe.com/reaction/1716322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Fluoro-benzenesulfonyl)-1-trityloxy-azepan-2-oneHCID 68513693—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product3-[4-(4-Methoxy-phenoxy)-benzenesulfonyl]-1-trityloxy-azepan-2-oneHCID 68516340—

Reaction Conditions

Temperature100 °C

Reaction Steps

A Mixture of 3-(4-fluoro-benzenesulfonyl)-1-trityloxy-azepan-2-one prepared from step F (18.9 mg, 0.0357 mmol), 4-methoxy-phenol (19.2 mg, 0.154 mmol) and K2CO3 (38.1 mg, 0.275 mmol) in anhydrous DMA (1.5 mL) was stirred and heated at 100° C. for overnight. The reaction mixture was diluted with EtOAc and washed sequentially with water and saturated NaCl solution. The organic phase was then dried over anhydrous Na2SO4 and concentrated under reduced pressure to gave a crude material, which was then purified by a column chromatography (0˜25% EtOAc in hexane). MS: 656.5 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803793B2
Source datasetuspto-grants-2010_09
ORD IDord-37e6fe15b55f43ab91300e09decc8e94
Source noteuspto-grants-2010_09