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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400369Generated: November 3, 2026

Trimethylsilyl triflate → 3-Bromo-4-oxo-piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/2400369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl triflateHCID 65367—
ReactantN-bromobutanimideHCID 67184—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
SolventDichloromethaneHCID 6344—
Product3-Bromo-4-oxo-piperidine-1-carboxylic acid benzyl esterHCID 2240700290%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796262B2
Source datasetuspto-grants-2014_08
ORD IDord-25bc39fe37584ade960db3d7f13e6154
Source noteuspto-grants-2014_08