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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382708Generated: October 31, 2026

Hydrochloric Acid → HCID 22725142, compound

https://huagongshe.com/reaction/382708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22725185HCID 22725185—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22725142HCID 2272514243%

Reaction Steps

To a stirred solution of 3-[4-(4-methoxyphenyl)-4-phenylpiperidin-1-yl]propionitrile (1.41 g, 4.40 mmol, 1.0 equiv) in anhydrous THF (10 mL) under argon was added a solution of BH3 in THF (1.0 M, 11.0 mL, 2.5 equiv) at room temperature. The mixture was refluxed for 4.5 hours and then cooled to room temperature. Aqueous HCl (6 N, 15 mL) was added and stirring was continued for 2 hours at 55-60° C. The mixture was basified to pH 9 by addition of 6 N aqueous NaOH and extracted with CH2Cl2 (3×75 mL). The combined organic solutions were dried over MgSO4 and concentrated. The residue was dissolved in CH2Cl2 (10 mL) and treated with HCl in ether (1.0 M, 9.0 mL, 2.0 equiv). The solvents were removed, ether (30 mL) was added, the mixture was filtered, and the filter cake was washed with ether (2×10 mL). Water (20 mL) was added to the resulting white solid, the pH was adjusted to 10 with 1 M NaOH, and the aqueous phase was extracted with CH2Cl2 (3×40 mL). The combined organic solutions were dried over MgSO4 and concentrated to give 610 mg (43%) of white solid, which was characterized spectroscopically.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310076B1
Source datasetuspto-grants-2001_10
ORD IDord-bf0236609aaf4b2f93c196c8c782eabc
Source noteuspto-grants-2001_10