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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909668Generated: October 30, 2026

4-Phenoxyphenol → HCID 69003419, compound

https://huagongshe.com/reaction/1909668

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) in 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 rt 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 numberUS08598359B2
Source datasetuspto-grants-2013_12
ORD IDord-5ec02f0f8be4447b8d25c9e8b29017b8
Source noteuspto-grants-2013_12