HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658297Generated: October 26, 2026
Hydrochloric Acid → 4-[1-Allyl-1-(2,6-dimethyl-4'-trifluoromethyl-biphenyl-4-yloxymethyl)-but-3-enyl]-benzoic acid
https://huagongshe.com/reaction/658297
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4-[1-Allyl-1-(2,6-dimethyl-4'-trifluoromethyl-biphenyl-4-yloxymethyl)-but-3-enyl]-benzoic acid methyl ester | HCID 67485717 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[1-Allyl-1-(2,6-dimethyl-4'-trifluoromethyl-biphenyl-4-yloxymethyl)-but-3-enyl]-benzoic acid | HCID 68489436 | 95% |
Reaction Steps
A solution of 4-[1-allyl-1-(2,6-dimethyl-4′-trifluoromethyl-biphenyl-4-yloxymethyl)-but-3-enyl]-benzoic acid methyl ester (0.386 g, 0.758 mmol) in THF (8.0 mL) is treated with 1N LiOH (8.0 mL, 8.0 mmol), warmed to 70° C., and stirred overnight. The reaction mixture is cooled to room temperature, acidified with 1N HCl (9.0 mL), and extracted with EtOAc (3×20 mL). The combined extracts are dried over MgSO4, filtered, and concentrated to provide 0.356 g (95%) of the title compound as a white foam. MS (ES): 493.3 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076374B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-d4fe546a8eaa4ddbae659d178d33d9ad |
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| Source note | uspto-grants-2011_12 |
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