HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848873Generated: October 26, 2026
Methyl 2,4-Difluorobenzoate → Methyl 2-(6-(benzyloxy)pyridin-3-yloxy)-4-fluorobenzoate
https://huagongshe.com/reaction/1848873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2,4-Difluorobenzoate | HCID 2782897 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 6-(Benzyloxy)pyridin-3-ol | HCID 42553041 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(6-(benzyloxy)pyridin-3-yloxy)-4-fluorobenzoate | HCID 67228431 | — |
Reaction Steps
To 6-(benzyloxy)pyridin-3-ol (1.10 g) in 2-methyltetrahydrofuran (20 mL) was added potassium t-butoxide (5.47 mL, 1.0M in tetrahydrofuran). After stirring for 15 minutes, methyl 2,4-difluorobenzoate (1.035 g) in 2-methyltetrahydrofuran (2 mL) was added and the reaction heated to 75° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (150 mL), washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (SF40-80 g) eluting with a gradient of 5% to 20% ethyl acetate/hexanes gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952157B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-c0c383a1b3694a4ca38a87e534d3846e |
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| Source note | uspto-grants-2015_02 |
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