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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443273Generated: October 30, 2026

m-Xylyl bromide → HCID 21193326, compound

https://huagongshe.com/reaction/443273

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Xylyl bromideHCID 12099—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant4-Benzyl 1-tert-butyl piperidine-1,4-dicarboxylateHCID 22255913—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21193326HCID 21193326—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cold (-78° C.) solution of benzyl N-tert-butoxycarbonyl-isonipecotate (8.02 g, 25.11 mmol) in anhydrous THF (80 mL), a solution of sodium bis(trimethysilyl)amide (35 mL, 35 mmol; 1M) in THF was added over a period of 10 min. The resulting orange solution was stirred at -78° C. for 1 h. and then treated dropwise with 3-methylbenzyl bromide (4.1 mL, 30.6 mmol). The reaction mixture was allowed to warm to room temp., and stirred overnight. The reaction was quenched with saturated aqueous ammonium chloride, diluted with water, and extracted with ethyl acetate. The organic extracts were combined, washed with brine, and concentrated under vacuum. The residual oil was subjected to column chromatography on silica eluting with 20% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-f64c3a42dfd44820bd1b4599428ee5a2
Source noteuspto-grants-1999_04