HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966274Generated: October 30, 2026
Ethyl Acetate → Methyl 2-(2-benzyloxy-4-fluorophenyl)-3-methyl-5-nitrobenzoate
https://huagongshe.com/reaction/1966274
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Benzyloxy-4-fluorophenylboronic acid | HCID 2782665 | — |
| Reactant | Methyl 3-methyl-5-nitro-2-trifluoromethylsulfonyloxybenzoate | HCID 58026836 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 2-(2-benzyloxy-4-fluorophenyl)-3-methyl-5-nitrobenzoate | HCID 58026740 | 70% |
Reaction Steps
A mixture of methyl 3-methyl-5-nitro-2-trifluoromethylsulfonyloxybenzoate (Reference Compound No. 1-4-(3), 13.26 g, 38.6 mmol), 2-benzyloxy-4-fluorophenylboronic acid (14.3 g, 58.1 mmol), potassium phosphate (21.3 g, 100 mmol) and tetrakis(triphenylphosphine)palladium(0) (3.23 g, 2.80 mmol) was suspended in anhydrous 1,4-dioxane (200 mL), and then the mixture was refluxed for 3 days. After cooling down, ethyl acetate (500 mL) was added thereto, and then the whole was washed with water (500 mL) and saturated brine (50 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (10.7 g) as a pale brown solid. (Yield 70%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420635B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-805872016d284dafaabd1f88b66e5c40 |
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| Source note | uspto-grants-2013_04 |
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