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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249449Generated: October 29, 2026

Hydrochloric Acid → HCID 70228308, compound

https://huagongshe.com/reaction/249449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 45264923HCID 45264923—
SolventWaterHCID 962—
ProductHCID 70228308HCID 7022830852%

Reaction Steps

1-[2-[[2-(3-Methoxyphenyl)-2-(2-methylphenyl)ethenyl]oxy]-ethyl]-1, 2,5,6-tetrahydro-3-pyridine carboxylic acid methyl ester (1.15 g, 0.0027 mol) (prepared as described in Method D) was dissolved in ethanol (15 ml) and 12 N sodium hydroxide solution (0.5 ml) was introduced. After stirring the solution at room temperature for 4 h, ice (30 g) was added, and the pH of the reaction mixture was adjusted to ca. 7 with 37% hydrochloric acid solution. Dichloromethane (200 ml) was added, and the pH was further adjusted to ca. 1 with 37% hydrochloric acid solution. Water was added until the solid material was dissolved, and the dichloromethane phase was dried (Na2SO4) and evaporated to an oil, which was co-evaporated three times with acetone. The residue was triturated with diethyl ether to give the title compound (0.60 g, 52%), which gave HPLC retention times of 17.1 and 17.6 min. for the geometric isomers (gradient elution, water/20-80% acetonitrile, both containing 0.1% TFA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214057
Source datasetuspto-grants-1993_05
ORD IDord-c767c35253d34105ade0b6cd8bbc4b23
Source noteuspto-grants-1993_05