HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496702Generated: October 31, 2026
Potassium Carbonate → HCID 89961841, compound
https://huagongshe.com/reaction/1496702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Difluorobenzyl bromide | HCID 518896 | — |
| Reactant | 3-Methylpyrrolidin-3-ol hydrochloride | HCID 53346559 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 89961841 | HCID 89961841 | — |
Reaction Steps
According to Example 15, 3-methylpyrrolidin-3-ol hydrochloride was synthesized. To a 100 mL reaction flask were added 3-methylpyrrolidin-3-ol hydrochloride (1 g, 7.2 mmol), anhydrous potassium carbonate (2.5 g, 18 mmol) and acetonitrile (15 mL). To the resulting mixture was slowly added a solution of 3,5-difluorobenzyl bromide (1.64 g, 7.9 mmol) in acetonitrile dropwisely at 85° C. The reaction was conducted for 12 hours. After the completion of reaction monitored by TLC, the resulting mixture was evaporated under reduced pressure to remove acetonitrile. To the residue was added a mixed solution of dichloromethane and water for extraction. The organic phase was dried over anhydrous sodium sulfate, and evaporated to remove the solvent to produce a crude product of 1-(3,5-difluorobenzyl)-3-methylpyrrolidin-3-ol (1.8 g), which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09198902B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-5f51e6eae93d4f0eaf21bb1fb54a7aa1 |
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| Source note | uspto-grants-2015_12 |
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