HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910511Generated: October 27, 2026
1,2-Dichloroethane → (3,4-Difluorophenyl)(phenyl)methyl quinuclidine-3-carboxylate
https://huagongshe.com/reaction/1910511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | (3,4-Difluorophenyl)(phenyl)methanol | HCID 2758251 | — |
| Reactant | 1-Azabicyclo(2.2.2)octane-3-carboxylic acid hydrochloride | HCID 12673436 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3,4-Difluorophenyl)(phenyl)methyl quinuclidine-3-carboxylate | HCID 70925855 | 43.3% |
Reaction Steps
Quinuclidine-3-carboxylic acid hydrochloride (80 mg, 0.42 mmol), EDC (120 mg, 0.62 mmol), and HOBT (96 mg, 0.62 mmol) were dissolved in dry THF (3 ml). (3,4-Difluorophenyl)(phenyl)methanol (101 mg, 0.46 mmol) was dissolved in dry THF (2 ml) and then added to the reaction mixture. Triethylamine (203 μl, 1.46 mmol) was finally added, and the resulting reaction was stirred at room temperature overnight. The volatiles were evaporated, and the crude was taken up with EtOAc and washed with water and then with sat. NaHCO3. The organic phase was dried over sodium sulfate, filtered, and evaporated under vacuum. The crude was purified by flash chromatography (DCM/MeOH=9/1) to obtain (3,4-difluorophenyl)(phenyl)-methyl quinuclidine-3-carboxylate (65 mg, mixture of diastereoisomers).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604015B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-c0f7c0dcb0224b5ca311e8403c7d6e60 |
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| Source note | uspto-grants-2013_12 |
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