HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505446Generated: October 30, 2026
4-Methoxybenzoic Acid → HCID 68659330, compound
https://huagongshe.com/reaction/505446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzoic Acid | HCID 7478 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Benzoic acid, 3-fluoro-, ethyl ester | HCID 67975 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Product | HCID 68659330 | HCID 68659330 | — |
Reaction Steps
s-Butyllithium (52 mL, 1.4 M in pentane, 72 mmol) was added at −78 C over 90 min. to a solution of p-Anisic acid (5 g, 33 mmol) and TMEDA (11 ml, 72 mmol) in THF (80 mL). After stirring for 15 min. ethyl 3-fluorobenzoate (5 mL, 40 mmol) was added in one portion. The reaction mixture was stirred for 15 min. then it was quenched with water (20 mL). The reaction mixture was then warmed to room temperature poured into water (1.5 L) 1N NaOH (30 ml) was added and the reaction mixture was then extracted with EtOAc. The extracts were discarded. The aqueous phase was then acidified with conc. HCl to pH 1 and extracted with EtOAc. Drying (Na2SO4) and concentration gave a residue which was recrystallized from hexanes/EtOAc to give the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07781457B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-1764eb1921964e0188df4702d06cc015 |
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| Source note | uspto-grants-2010_08 |
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