HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044869Generated: October 26, 2026
Carbon tetrabromide → Benzyl 2-(3-bromopropyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1044869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzyl 2-(3-hydroxypropyl)piperidine-1-carboxylate | HCID 58306067 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 2-(3-bromopropyl)piperidine-1-carboxylate | HCID 58306190 | 81.1% |
Reaction Steps
To a solution of phenylmethyl 2-(3-hydroxypropyl)-1-piperidinecarboxylate (2.14 g, 7.72 mmol) in anhydrous dichloromethane (34 ml) was added carbon tetrabromide (5.12 g, 15.43 mmol)). The resulting solution was cooled in ice/water. A solution of triphenylphosphine (4.05 g, 15.43 mmol) in 10 ml dry DCM was added dropwise over 30 mins., producing a deep amber/brown solution. After complete addition the reaction was allowed to warm slowly to ambient temperature and stirring continued overnight. The reaction mixture was filtered to remove the precipitate, washed with ether and the filtrate evaporated to approx 10 ml. This was then loaded onto a 100 g silica cartridge and purified by chromatography using a gradient of Flashmaster 0-25% ethylacetate in cyclohexane over 40 mins. on a Flashmaster collecting all the eluent. The product peak was identified by TLC and the fractions combined and evaporated in vacuo to give the title compound as a clear oil (2.13 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-5690d6003b084858a3bd688f64e3bc79 |
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| Source note | uspto-grants-2013_10 |
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