HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864000Generated: November 1, 2026
Cyclohexane → (S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1864000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | tert-Butyl (3S)-3-(hydroxymethyl)piperidine-1-carboxylate | HCID 1514448 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate | HCID 34177035 | 91% |
Reaction Steps
To a solution of 1,1-dimethylethyl (3S)-3-(hydroxymethyl)-1-piperidinecarboxylate (30.0 g, 139 mmol) and carbon tetrabromide (72.0 g, 217 mmol) in methylene chloride (150 mL) was added dropwise a solution of triphenyl phosphine (42.4 g, 162 mmol) in methylene chloride (150 mL). An ice-bath was used to maintain an internal temperature between 20 and 25° C. during the addition. After stirring the mixture at ambient temperature for 1 h, cyclohexane (500 mL) was added. Approximately one-half of the solvent was removed under reduced pressure. The remaining solution was cooled in an ice bath and the resulting precipitate was removed by filtration. The filtrate was concentrated under reduced pressure and the residue subjected to flash chromatography (0% to 25% ethyl acetate/hexanes, silica gel) to give 35.1 g (91% yield) of the desired product as a solid. MS (ES+) m/z 278 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625890B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-6649e41ae8554d88b45db195e9a9556a |
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| Source note | uspto-grants-2009_12 |
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