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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250230Generated: November 3, 2026

alpha-Bromo-2-nitrotoluene → HCID 54074348, compound

https://huagongshe.com/reaction/2250230

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Bromo-2-nitrotolueneHCID 77569—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant1-Tert-butyl 4-ethyl piperidine-1,4-dicarboxylateHCID 2758812—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54074348HCID 5407434813%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (8.23 g, 0.032 mol) in tetrahydrofuran (85 mL) was slowly added a solution of sodium bis(trimethylsilyl)amide (44 mL, 0.044 mol). After the resulting mixture had been stirred at −78° C. for 1 h, a solution of 2-nitrobenzyl bromide (8.21 g, 0.038 mol) was added. The reaction mixture was allowed to warm up to room temperature and was stirred overnight. It was then concentrated and the residue was partitioned between water and ethyl acetate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The final product was purified from the complex reaction mixture by way of column chromatography on silica gel (eluent—hexanes-ethyl acetate 4:1) to give the desired product (1.61 g, 13%) as brown oil. Mass spec.: 415.38 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314883B2
Source datasetuspto-grants-2008_01
ORD IDord-a48aa0a2138e40cdbaa8bcd3ab211c4e
Source noteuspto-grants-2008_01