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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259925Generated: November 2, 2026

Hydrochloric Acid → HCID 67714944, compound

https://huagongshe.com/reaction/2259925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl oxalateHCID 11120—
ReactantSodium hydrideHCID 24758—
ReactantN-Benzyl-4-Acetyl4-(4-Chlorobenzyl)-piperidineHCID 19962174—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 67714944HCID 6771494450.8%

Reaction Steps

A solution of N-Benzyl-4-Acetyl-4-(4-Chlorobenzyl)piperidine (600 mg, 1.75 mmol) and dimethyl oxalate (310 mg, 2.63 mmol) in dimethoxyethane (20 mL) was treated with sodium hydride (105 mg of a 60% dispersion in mineral oil, 2.63 mmol) and heated to reflux for 3 hours. The reaction was then cooled to room temperature, poured into 1N aqueous HCl (200 mL) and extracted with ethyl ether (1×50 mL). The ether extract was discarded. The pH of the aqueous phase was adjusted to pH 8 and extracted with ethyl acetate (3×200 mL). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated at reduced pressure. The crude ester thus obtained was dissolved in THF (5 mL) and 3N HCl (20 mL) and heated to reflux for 1 hour. The reaction was then cooled to room temperature, and concentrated at reduced pressure. The residue was triturated with tetrahydrofuran and the solid collected by filtration and crystallized from isopropanol to give 200 mg of the title compound. mp. 189°-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05475109
Source datasetuspto-grants-1995_12
ORD IDord-e7ae1e0935c246f896317ecbbad6d597
Source noteuspto-grants-1995_12