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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173737Generated: October 31, 2026

Hydrochloric Acid → HCID 178507695, compound

https://huagongshe.com/reaction/2173737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetonitrileHCID 6342—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium hydrideHCID 24758—
Reactant1-Piperidineacetic acid, ethyl esterHCID 643466—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178507695HCID 178507695—

Reaction Conditions

Temperature80 °C

Reaction Steps

NaH (0.234 g, 5.84 mmol) in dry toluene (5 ml) was heated to 80° C. A mixture of acetonitrile (0.229 ml, 4.38 mmol), ethyl 1-piperidineacetate (0.5 g, 2.92 mmol) and toluene (3 ml) was added dropwise to the hot reaction mixture. The mixture was stirred at 80° C. for 1.5 hours and after cooling to RT, quenched by the addition of water (6 ml). Hydrazine hydrate (0.142 ml, 2.92 mmol) was added and reaction mixture reheated to 80° C. for 3 hours. The reaction mixture was acidified with 2N HCl (aq.) to pH 2 and loaded onto a SCX-2 cartridge eluting with MeOH followed by 7M NH3 in MeOH. The methanolic ammonia fractions were concentrated in vacuo to afford an oil. 4N HCl in dioxane (15 ml) was added to the yellow oil and the resulting suspension was filtered and washed with iso-hexane to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056867B2
Source datasetuspto-grants-2015_06
ORD IDord-8bc0a6042efa4edbad0a91f1430644a7
Source noteuspto-grants-2015_06