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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055882Generated: November 1, 2026

Hydrochloric Acid → 4-(2,3-Dimethoxybenzoyl)piperidine

https://huagongshe.com/reaction/2055882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantN-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanoneHCID 46780868—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(2,3-Dimethoxybenzoyl)piperidineHCID 2273784965%

Reaction Conditions

Temperature60 °C

Reaction Steps

To the reaction solution of 4-(2,3-dimethoxybenzoyl)-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (7) from Example 76, Scheme G, step c, is added about 188 kg of water and 37% hydrochloric acid (39 kg, 395 mol). The solution is heated to about 60° C. for about 18 hours1. The mixture is cooled to about 25° C. and about 47 kg of toluene is added. The phases are separated and the organic phase is discarded. To the aqueous phase is added about 78 kg water, 50 wt % sodium hydroxide solution (31 kg, 391 mol), and about 99 kg of toluene. The phases are separated and the aqueous phase is discarded. The organic phase is concentrated by vacuum distillation. The concentration of 4-(2,3-dimethoxybenzoyl)piperidine (16) in solution ranges from 17 to 53 wt %1, affording 14.6 to 17.9 kg of 4-(2,3-dimethoxybenzoyl)piperidine (16) (65-76% yield). 1The solution is sampled and analyzed by HPLC assay to confirm complete deprotection to afford 4-(2,3-dimethoxybenzoyl)piperidine (16). The reaction is complete if less than 5 area % of 4-(2,3-dimethoxybenzoyl)-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (7) is detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332607B2
Source datasetuspto-grants-2008_02
ORD IDord-76f5b7fc694f404aa9411b2b18b6cf3b
Source noteuspto-grants-2008_02