HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943556Generated: October 27, 2026
Hydrochloric Acid → 4-Ethoxy-2,3-difluoro-4'-biphenylbenzoic acid
https://huagongshe.com/reaction/1943556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-ethoxy-2,3-difluoro-4'-biphenylbenzoate | HCID 66682456 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Ethoxy-2,3-difluoro-4'-biphenylbenzoic acid | HCID 67082370 | 48.2% |
Reaction Steps
The compounds (3) (29.1 g), sodium hydroxide (11.4 g), Solmix A-11 (100 ml) and water (100 ml) were mixed, and the mixture was heated under reflux for 2 hours. The reaction mixture was cooled to 30° C., and then aqueous 6N-hydrochloric acid solution (100 ml) and toluene (200 ml) were added hereto and mixed. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases, and extraction into an organic phase was carried out. The organic phase obtained was fractionated, washed sequentially with water, a saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate, giving 13.0 g of 4-ethoxy-2,3-difluoro-4′-biphenylbenzoic acid (44). The yield based on the compound (3) was 49.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394294B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-5480e426a06b488cae572174ad93f673 |
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| Source note | uspto-grants-2013_03 |
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