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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254001Generated: November 2, 2026

N-bromobutanimide → HCID 58179516, compound

https://huagongshe.com/reaction/254001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58179661HCID 58179661—
SolventAcetonitrileHCID 6342—
ProductHCID 58179516HCID 5817951623.1%

Reaction Steps

N-Bromosuccinimide (4.9 g, 28.08 mmol) was added in portions to a solution of tert-butyl 4-(thiophen-2-yl)piperidine-1-carboxylate (5.0 g, 18.72 mmol) in MeCN at −10° C. The reaction mixture was stirred for 30 minutes and treated with sat. aq. NaHCO3 solution. The mixture was extracted with CH2Cl2 and the organics washed with water and brine solution, dried (Na2SO4), filtered, and evaporated to obtain crude product. Purification by silica gel chromatography (2% EtOAc/pet ether) yielded tert-Butyl 4-(5-bromothiophen-2-yl)piperidine-1-carboxylate (1.5 g, 21% from tert-butyl 4-hydroxy-4-(thiophen-2-yl)piperidine-1-carboxylate); 1H-NMR (400 MHz, CHCl3): 6.85 (d, 1H), 6.58 (d, 1H), 4.22-4.10 (d, 2H), 3.90-3.78 (m, 3H), 1.98-1.90 (d, 2H), 1.65-1.48 (m, 2H), 1.45 (s, 9H); ES-MS: 346.3, 348.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872031B2
Source datasetuspto-grants-2011_01
ORD IDord-72d3189113234c09a22d0ea5b221e946
Source noteuspto-grants-2011_01