Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | Tetrahydro-3-furanmethanol | HCID 139980 | — |
| Reactant | Methyl 4-fluorosalicylate | HCID 2775386 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66696256 | HCID 66696256 | 70% |
Reaction Steps
To a solution of 3 g of methyl 4-fluoro-2-hydroxybenzoate in 60 mL of tetrahydrofuran were added 1.98 g of tetrahydrofuran-3-ylmethanol and 4.28 g of tributylphosphine, followed by ice-cooling. To a mixture was gradually added 6.67 g of 1,1′-(azodicarbonyl)dipiperidine, followed by stirring for 20 minutes. The mixture was warmed to room temperature, stirred for 16 hours, and then poured into a mixture of water and ethyl acetate. The aqueous layer was separated, the organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain 3.14 g of methyl 4-fluoro-2-(tetrahydrofuran-3-ylmethoxy)benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901126B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-96a967d31ef04a72a2cb2983509ea9ad |
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| Source note | uspto-grants-2014_12 |
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