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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985482Generated: October 28, 2026

Toluene → Tert-butyl 4-(1-methoxy-3-(2-nitrophenyl)-1-oxopropan-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1985482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactantalpha-Bromo-2-nitrotolueneHCID 77569—
Reactanttert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylateHCID 1514280—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(1-methoxy-3-(2-nitrophenyl)-1-oxopropan-2-yl)piperidine-1-carboxylateHCID 5973204141%

Reaction Conditions

Temperature-78 °C

Reaction Steps

tert-Butyl 4-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate (240 mg, 0.93 mmol) was dissolved in tetrahydrofuran (7 mL). Mixture was cooled to −78° C. A 0.5 M solution of potassium bistrimethylsilyl)amide in toluene (2.2 mL, 1.1 mmol) was added to the mixture drop-wise. Reaction stirred at −78° C. for 20 minutes. A solution of 2-nitrobenzylbromide (240 mg, 1.1 mmol) in tetrahydrofuran (2 mL) was added to the reaction mixture drop-wise. Reaction stirred at −78° C. for 40 minutes. Dry ice bath was removed and the reaction mixture was allowed to warm to room temperature over 30 minutes. Reaction was quenched with aqueous ammonium chloride. Mixture was extracted with ethyl acetate (2×20 mL). Combined extracts were dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography afforded the title compound as yellow oil in 41% yield. MS m/e (M−C4H8+H)+=337.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544680B2
Source datasetuspto-grants-2009_06
ORD IDord-cf6f566d8b9d48e3af3d9a43dc74f5da
Source noteuspto-grants-2009_06