HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424690Generated: October 29, 2026
Carbon Dioxide → 2-Fluoro-3-methoxybenzoic acid
https://huagongshe.com/reaction/424690
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2-Fluoroanisole | HCID 67576 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Fluoro-3-methoxybenzoic acid | HCID 3390679 | — |
Reaction Steps
Pentamethylenediethylenetetramine (31.2 ml) was added to a solution of 2-fluoroanisole (15.0 g) in THF (450 ml). The reaction mixture was cooled to −78° C. and n-butyllithium (59.6 ml, 2.5M solution in hexanes) was added dropwise. Stirring was maintained for 2 h before the solution was added in a dropwise fashion to a flask containing solid carbon dioxide pellets. Upon complete addition (30 min) the mixture was allowed to warm to room temperature before removal of the volatiles in vacuo. The residue was dissolved in 10% sodium hydroxide solution (300 ml) and extracted with Et2O (3×). The aqueous was acidified to pH 1 with concentrated hydrochloric acid before extracting with DCM. The organics were washed with H2O, dried (MgSO4) and concentrated in vacuo to afford the subtitle compound as a yellow solid. Yield: 7.1 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106063B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-7bf291c6512e483fac443a9db0564a00 |
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| Source note | uspto-grants-2012_01 |
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