HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044865Generated: October 31, 2026
Carbon tetrabromide → Benzyl 2-(2-bromoethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1044865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzyl 2-(2-hydroxyethyl)piperidine-1-carboxylate | HCID 45358666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 2-(2-bromoethyl)piperidine-1-carboxylate | HCID 58306210 | 74.1% |
Reaction Steps
To a solution of phenylmethyl 2-(2-hydroxyethyl)-1-piperidinecarboxylate (1.76 g, 6.70 mmol) in anhydrous dichloromethane (29 mL) was added carbon tetrabromide (4.44 g, 13.39 mmol). The resulting solution was cooled in ice/water. A solution of triphenylphosphine (1.76 g, 6.70 mmol) in 10 ml dry DCM was added dropwise over 30 mins. After complete addition the reaction was allowed to warm slowly to ambient temperature and stirring continued overnight. The reaction solution was reduced in volume to <10 ml (opaque) and this was loaded onto a 100 g silica cartridge and purified by chromatography on a Flashmaster 2 using a gradient of 0-25% ethyl acetate in cyclohexane over 40 minutes. Product fractions were combined and evaporated in vacuo to give the title compound as a colourless oil (1.62 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563717B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-3dfef07b9c1d42f687a11f6803d7a206 |
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| Source note | uspto-grants-2013_10 |
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