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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964243Generated: October 30, 2026

Hydrochloric Acid → HCID 2235157, compound

https://huagongshe.com/reaction/964243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantHCID 23004105HCID 23004105—
SolventTetrahydrofuranHCID 8028—
ProductHCID 2235157HCID 223515791%

Reaction Steps

To a stirred solution of 3-(4-benzylpiperidin-1-yl)propionitrile (8.20 g, 35.9 mmol, 1.0 equiv) in anhydrous THF (20 mL) under argon was added a solution of BH3 in THF (1.0M, 126 mL, 3.5 equiv) at room temperature. The mixture was refluxed for 4.5 hours, then cooled to room temperature and concentrated to a volume of about 30 mL. Aqueous HCl (6 N, 80 mL) was added and stirring was continued for 2 hours at 55°-60° C. The mixture was basified to pH 9 by addition of 6N aq. NaOH and extracted with CH2Cl2 (3×150 mL). The combined organic solutions were dried over MgSO4 and concentrated. The residue was dissolved in CH2Cl2 (20 mL) and treated with HCl in ether (1.0M, 75 ml, 2.1 equiv). The solvents were removed, ether (60 mL) was added, the mixture was filtered, and the filter cake was washed with ether (2×30 mL). Water (40 mL) was added to the resulting white solid, the pH was adjusted to 10 with 1M NaOH, and the aqueous phase was extracted with CH2 Cl2 (3×80 mL). The combined organic solutions were dried over MgSO4 and concentrated to give 7.59 g (91%) of colorless oil, which was characterized spectroscopically.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767131
Source datasetuspto-grants-1998_06
ORD IDord-1da655eae3a249028dc1052367c27abf
Source noteuspto-grants-1998_06