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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055871Generated: October 29, 2026

Veratrole → N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanone

https://huagongshe.com/reaction/2055871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVeratroleHCID 7043—
Reactant4-(Methoxymethylcarbamoyl)piperidine-1-carboxylic acid tert-butyl esterHCID 44203202—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductN-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanoneHCID 46780868—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of n-BuLi (2.5M, 452 mL) in hexane was added to a solution of veratrole (149 g, 1.08 mol) in anhydrous tetrahydrofuran (1.2 L) over 10 minutes at −78° C. under nitrogen. The resulting solution was stirred at 0° C. for 1 hour and room temperature for 4 hours. A solution of 4-[(methoxymethylamino)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (15) (275 g, 1.01 mol) in tetrahydrofuran (800 mL) was added to the reaction slurry at −65° C. over 20 minutes. The mixture was warmed to room temperature, stirred for 18 hours and quenched with saturated ammonium chloride (1 L). After stirring for 1 hour, the phases were separated and the aqueous layer was extracted with ethyl ether (1 L). The combined organic solutions were washed with brine (2 L) and dried (MgSO4). The mixture was filtered and the filtrate was concentrated (30° C./20 torr) to a residue (413 g). The solution may be used directly in Scheme L, step a, Example 108.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332607B2
Source datasetuspto-grants-2008_02
ORD IDord-1afff0c149c84495ad5a9053ec035926
Source noteuspto-grants-2008_02