HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538451Generated: October 26, 2026
1,2-Dibromoethane → Tert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylate
https://huagongshe.com/reaction/538451
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Tert-butyl 4-(4-bromobenzyl)-4-hydroxypiperidine-1-carboxylate | HCID 70851437 | 40.4% |
Reaction Steps
To a suspension of magnesium (2.9 g) in diethyl ether (50 mL) was added dropwise 1,2-dibromoethane (0.90 mL) at room temperature, and the reaction mixture was vigorously stirred at room temperature for 20 min. To the reaction mixture was added dropwise a solution of 4-bromobenzyl bromide (25 g) in diethyl ether (150 mL) over 30 min or more at 0° C., and then added dropwise a solution of tert-butyl 4-oxopiperidine-1-carboxylate (16 g) in diethyl ether (200 mL) over 30 min or more 0° C. The reaction mixture was allowed to warm to room temperature, and stirred at room temperature for 3 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution (200 mL), and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (12 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08865717B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-24880964c55a49b5bcb5614bea537266 |
|---|
| Source note | uspto-grants-2014_10 |
|---|