HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908088Generated: November 3, 2026
Triphenylphosphine → HCID 58551520, compound
https://huagongshe.com/reaction/1908088
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl Vanillate | HCID 19844 | — |
| Reactant | (S)-(+)-3-Hydroxytetrahydrofuran | HCID 2733227 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58551520 | HCID 58551520 | 84.1% |
Reaction Steps
To a stirred solution of (3S)-tetrahydrofuran-3-ol (403 mg, 4.57 mmol), methyl 4-hydroxy-3-methoxy-benzoate (1.00 g, 5.49 mmol) and triphenylphosphane (1.44 g, 1.27 mL, 5.49 mmol) in THF (13 mL) at 0° C. was added DIAD (1.11 g, 1.06 mL, 5.49 mmol). The ice bath was removed and the reaction mixture was stirred at room temperature for 16 h, then at 55° C. for 4 h. The mixture was diluted with EtOAc and was washed with sat. aq. NaHCO3 (×2) and brine (×2). The organic layer was dried over Na2SO4, filtered and the solvent was evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel (0-30% ethyl acetate in hexane) to yield (R)-methyl 3-methoxy-4-(tetrahydrofuran-3-yloxy)benzoate (0.97 g, 84%) as a viscous liquid. ESI-MS m/z calc. 252.1. found 253.3 (M+1)+; Retention time: 1.72 minutes (3 min run).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598164B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-df1a697c0c7f4de79c890eb9042a8520 |
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| Source note | uspto-grants-2013_12 |
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