HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530978Generated: October 31, 2026
Tetrahydrofuran → 2-Cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carbaldehyde
https://huagongshe.com/reaction/530978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 2-cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carboxylate | HCID 90423848 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Cyclopropyl-6-ethoxy-4'-fluorobiphenyl-4-carbaldehyde | HCID 90423588 | 85.7% |
Reaction Steps
A THF (50 mL) solution of ethyl 2-cyclopropyl-6-ethoxy-4′-fluorobiphenyl-4-carboxylate (10.5 g) was added to a THF (50 mL) suspension of lithium aluminum hydride (1.21 g) under ice cooling in a nitrogen atmosphere. After stirring at the same temperature as above for 30 minutes, water (1.2 mL) and a 15% aqueous sodium hydroxide solution (1.2 mL) were added thereto, and the mixture was stirred for 5 minutes. Water (3.6 mL) was further added to the reaction mixture, and the mixture was stirred for 30 minutes and then filtered. The filtrate was concentrated under reduced pressure. Manganese dioxide (13.9 g) was added to a toluene (60 mL) solution of the obtained residue, and the mixture was stirred at 60° C. for 1 hour in a nitrogen atmosphere. The reaction mixture was filtered, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (7.79 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353108B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-4b8fad8525bf411f8689b17654ad2fad |
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| Source note | uspto-grants-2016_05 |
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