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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739011Generated: November 3, 2026

m-Xylyl bromide → HCID 54555641, compound

https://huagongshe.com/reaction/1739011

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Xylyl bromideHCID 12099—
ReactantSodium hydrideHCID 24758—
Reactant1-tert-Butyl 4-ethyl 3-oxopiperidine-1,4-dicarboxylateHCID 15852989—
SolventDimethylformamideHCID 6228—
ProductHCID 54555641HCID 54555641—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) slurry of sodium hydride (0.29 g, 12 mmol) in anhydrous dimethylformamide (50 mL), a solution of ethyl N-tert-butoxycarbonyl-3-oxo-piperidine-4-carboxylate (2.73 g, 10 mmol) in DMF (10 mL) was added. The mixture was stirred at 0° C. for 30 min., and at room temp. for 30 min. The resultant solution was cooled back to 0° C. and treated with 3-methylbenzyl bromide (1.63 mL, 12 mmol). The reaction mixture was stirred at room temp. overnight and concentrated under vacuum. The residue was partitioned between ethyl acetate and aqueous sodium bicarbonate. The organic extract was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 17.5% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965578
Source datasetuspto-grants-1999_10
ORD IDord-49ead2d6fee54f02a72f4df7869bc72f
Source noteuspto-grants-1999_10