HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510465Generated: November 2, 2026
Trimethylsilyl triflate → 3-Bromo-4-oxo-piperidine-1-carboxylic acid benzyl ester
https://huagongshe.com/reaction/510465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-4-oxo-piperidine-1-carboxylic acid benzyl ester | HCID 22407002 | 90% |
Reaction Steps
To a cooled (0° C.) solution of N-benzyloxycarbonyl-4-piperidone (501, 27.3 g 117 mmol) in DCM (3 ml/mmol) was added DIPEA (25.5 ml, 146.2 mmol, 1.25 eg) and trimethylsilyl trifluoromethane sulfonate (25.4 ml, 141 mmol, 1.2 eg). The mixture was stirred for 30 minutes at 0° C. Next, N-bromosuccinimide (21.2 g, 119.3 mml, 1.02 eg) was added and stirring was continued for 16 hrs at room temperature. The reaction mixture was washed with 5% NaHCO3 and the organic layer was dried (MgSO4) and subsequently concentrated under reduced pressure. The resulting oil was purified by silica gel chromatography (diethyl ether/petroleum ether, 1/1 to 1/0, v/v, Rf 0.1) giving 502 in a yield of 90% as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096612B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-e0afd907643a4545aad72c363d6c5065 |
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| Source note | uspto-grants-2015_08 |
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