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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749980Generated: October 30, 2026

4-Phenoxyphenol → HCID 69003419, compound

https://huagongshe.com/reaction/749980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenoxyphenolHCID 13254—
ReactantSodium hydrideHCID 24758—
Reactant(R)-tert-Butyl 2-((tosyloxy)methyl)pyrrolidine-1-carboxylateHCID 11760051—
SolventDimethylformamideHCID 6228—
ProductHCID 69003419HCID 6900341964.8%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of 4-phenoxyphenol (200 mg, 1.07 mmol) m DMF (3 mL) at 0-5° C. was added 60% NaH (75 mg, 1.875 mmol) at 0-5° C. The reaction mixture was stirred at rt for 15 min at 0-5° C. A solution of (R)-2-(Toluene-4-sulfonyloxymethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (382 mg, 1.074 mmol) in DMF (2 mL) was added to the above mixture at 0-5° C. The reaction mixture was warmed to it and then heated at 90° C. for 15 h. The mixture was concentrated, diluted with saturated aq NaHCO3 and extracted with ethyl acetate. The aqueous layer was re-extracted with ethylacetate. The combined organic layers were dried over anhy. MgSO4 and the solvent was removed in vacuo to obtain the crude mixture, which was purified by silica gel flash chromatography to obtain the title product (256 mg, 64%); MS; m/z 370 (M+H) LCMS (UV)>90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402684B2
Source datasetuspto-grants-2008_07
ORD IDord-9d21cafcf0e94410b9ae023b6d542a0c
Source noteuspto-grants-2008_07