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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231714Generated: November 2, 2026

Hydrochloric Acid → HCID 14257855, compound

https://huagongshe.com/reaction/2231714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86742524HCID 86742524—
ReactantHCID 178418582HCID 178418582—
SolventEthanolHCID 702—
SolventEthylacetate methanolHCID 21584119—
ProductHCID 14257855HCID 14257855—

Reaction Steps

A solution of (4-methylphenyl)[1-(2-phenylethyl)-4-piperidinyl -methanone hydrochloride (9.5 g, 0.028 mol in absolute ethanol (350 ml) was treated first by the addition of NaOCH3 (1.62 g, 0.03 mol) and then, portionwise, with sodium borohydride (2.27 g, 0.06 mol) and stirred at room temperature for 18 h. The reaction mixutre was concentrated to a solid and stirred with 10% aqueous NaOH. The mixture was extracted with CH2Cl2 (3×50 ml). The CH2Cl2 solution was washed with water and then saturated NaCl solution, and dried over Na2SO4. After filtering off the Na2SO4, the filtrate was concentrated to a solid. This material was dissolved in EtOAc/Et2O (1:1, 200 ml) and treated with a solution of HCl 0.023 mol in CH3OH/EtOAc (3:10, 13 ml). The resulting precipitate was twice recrystallized from butanone containing a small amount of CH3OH to give alpha(4-methylphenyl)- 1-(2-phenylethyl)-4-piperidinemethanol hydrochloride, mp 181°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04783471
Source datasetuspto-grants-1988_11
ORD IDord-a7e0f9c3416e44f9a4fa49686cf0c494
Source noteuspto-grants-1988_11