HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623900Generated: October 30, 2026
Tetrahydrofuran → HCID 67975349, compound
https://huagongshe.com/reaction/623900
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 67975260 | HCID 67975260 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 67975349 | HCID 67975349 | 93.6% |
Reaction Steps
The mixture of 3-({4′-[1-benzyl-4-(trifluoromethyl)-1H-imidazol-2-yl]biphenyl-4-yl}oxy)-2,2-dimethylpropanoic acid (830 mg), 20% palladium hydroxide-carbon (850 mg) and tetrahydrofuran (20 mL) was stirred at 60° C. under hydrogen atmosphere for 6 hours. Nitrogen gas was passed through the reaction mixture, and the mixture was diluted with chloroform. The mixture was filtered by using a membrane filter, and the filtrate was washed with tetrahydrofuran, methanol and chloroform. The filtrates were combined, and n-hexane and propanol were added to the residue obtained by concentrating the same under the reduced pressure. The precipitated solid was collected by filtration to obtain 3-({4′-[5-(trifluoromethyl)-1H-imidazol-2-yl]biphenyl-4-yl}oxy)-2,2-dimethylpropanoic acid (635 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09302996B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-14d651d6b0e34d53bc5a422c8b229a21 |
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| Source note | uspto-grants-2016_04 |
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