HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749980Generated: October 30, 2026
4-Phenoxyphenol → HCID 69003419, compound
https://huagongshe.com/reaction/749980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (R)-tert-Butyl 2-((tosyloxy)methyl)pyrrolidine-1-carboxylate | HCID 11760051 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69003419 | HCID 69003419 | 64.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402684B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-9d21cafcf0e94410b9ae023b6d542a0c |
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| Source note | uspto-grants-2008_07 |
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