HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011787Generated: October 26, 2026
Potassium Carbonate → Methyl 3-[(phenylmethyl)oxy]-5-[(3S)-tetrahydrofuran-3-yloxy]benzoate
https://huagongshe.com/reaction/1011787
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-(benzyloxy)-5-hydroxybenzoate | HCID 7472028 | — |
| Reactant | Tetrahydrofuran-3-YL 4-methylbenzenesulfonate, (3R)- | HCID 11149197 | — |
| Solvent | Butyronitrile | HCID 8008 | — |
| Product | Methyl 3-[(phenylmethyl)oxy]-5-[(3S)-tetrahydrofuran-3-yloxy]benzoate | HCID 59127128 | 84.1% |
Reaction Steps
A mixture of methyl 3-hydroxy-5-{[phenylmethyl]oxy}benzoate (18.8 g, 72.75 mmol), (3R)-tetrahydrofuran-3-yl 4-methylbenzenesulfonate (18.5 g, 76.4 mmol) and potassium carbonate (20.08 g, 145.5 mmol) in butyronitrile (250 mL) was heated to 130° C. for 3 hours. The solvent was removed in vacuo and ethyl acetate added. The organics were washed with water (40 mL), 0.5M sodium hydroxide solution (40 mL), brine (40 mL), dried (MgSO4), filtered and the solvent removed in vacuo. The residue was chromatographed on silica, eluting with a gradient of 0-5% methanol in DCM, to give the desired compound as a colourless oil (20.1 g). 1H NMR δ (CDCl3): 2.08-2.26 (m, 2H), 3.78-4.01 (m, 4H), 3.90 (s, 3H), 4.92-4.96 (m, 1H), 5.08 (s, 2H), 6.69 (t, 1H), 7.15 (t, 1H), 7.29 (t, 1H), 7.34-7.44 (m, 5H); m/z 327 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977328B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-7a5dfc2a47434e0a8d53f12e13bd7afa |
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| Source note | uspto-grants-2011_07 |
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