HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539690Generated: October 25, 2026
Hydrochloric Acid → Tert-butyl 4-(3,4-difluorobenzyl)-4-hydroxypiperidine-1-carboxylate
https://huagongshe.com/reaction/539690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | 4-(Bromomethyl)-1,2-difluorobenzene | HCID 581436 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(3,4-difluorobenzyl)-4-hydroxypiperidine-1-carboxylate | HCID 86680862 | 59.6% |
Reaction Steps
To a suspension of magnesium (1.2 g) and 1,2-dibromoethane (0.11 mL) in diethyl ether (30 mL) was added a solution of 3,4-difluorobenzyl bromide (10 g) in diethyl ether (10 mL) at room temperature under a nitrogen atmosphere, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was diluted with THF (30 mL), and cooled to −78° C. A solution of tert-butyl 4-oxopiperidine-1-carboxylate (5.0 g) in THF (10 mL) was added thereto, and the mixture was allowed to warm to room temperature, and was stirred overnight. To the reaction mixture was added a small amount of 1N hydrochloric acid at 0° C. to quench the reaction. Saturated aqueous potassium sodium tartrate solution was added thereto, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane), and recrystallized from ethyl acetate/hexane to give the title compound (4.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871766B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-313a2d8d585047c8b67d6c06f4797822 |
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| Source note | uspto-grants-2014_10 |
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