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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249455Generated: October 29, 2026

Hydrochloric Acid → HCID 70228233, compound

https://huagongshe.com/reaction/249455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 70230542HCID 70230542—
SolventEthanolHCID 702—
ProductHCID 70228233HCID 70228233—

Reaction Steps

(R)-1-[3-[[2,2-bis(4-Fluorophenyl)ethenyl]oxy]propyl]-3-piperidine carboxylic acid ethyl ester tartrate (3.8 g, 0.0065 mol) (prepared as described in Method D) was dissolved in ethanol (25 ml) and 12 N sodium hydroxide solution (2.2 ml) was introduced at 5° After stirring the solution at room temperature for 4.8 h, the pH of the reaction mixture was adjusted to ca. 7 with 4 N hydrochloric acid solution, and the mixture was evaporated to a residue in vacuo. Water (25 ml) was added, and the mixture was extracted with dichloromethane (3 × 50 ml). The combined extacts were dried (MgSO4) and evaporated to a foam, which was dissolved in toluene (1.5 ml) and warmed to 40° Methanol (0.27 ml) was introduced followed by chlorotrimethylsilane (0.83 ml). The product precipitated slowly, and after the suspension had been allowed to stand for 18 h at room temperature it was collected by filtration. The title compound (2.9 g, quant.) was obtained as white crystals, m.p. 177°-180° (after drying in vacuo). HPLC retention time 12.55 (gradient elution, water/35-50% acetonitrile, aqueous phase containing 0.1 M ammonium sulphate solution).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05214057
Source datasetuspto-grants-1993_05
ORD IDord-be09feed98954f42bc0be79adb1ede21
Source noteuspto-grants-1993_05