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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483900Generated: October 31, 2026

Acetic Acid → 1-Sec-butyl-4-(3-methanesulfonyl-phenyl)piperidine

https://huagongshe.com/reaction/1483900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(3-(Methylsulfonyl)phenyl)piperidine hydrochlorideHCID 22397841—
Solvent1,2-DichloroethaneHCID 11—
Product1-Sec-butyl-4-(3-methanesulfonyl-phenyl)piperidineHCID 22397821—

Reaction Steps

4-(3-methanesulfonyl-phenyl)-piperidine hydrochloride (20 mg), glacial acetic acid (4.4 mg) and 2-butanone (5.1 mg) were mixed in 1,2-dichloroethane (5 mL). Sodium triacetoxyborohydride (23.5 mg) was added to the solution and the reaction mixture was stirred at room temperature under a nitrogen atmosphere for 5 h (G.L.C. analysis indicated a complete reaction). The reaction was quenched with saturated aqueous NaHCO3 and the product was extracted with CH2Cl2. The combined organic phases were dried (MgSO4), filtered, and the solvent was evaporated to afford 1-sec-butyl-4-(3-methanesulfonyl-phenyl)-piperidine as an oily residue. The product was chromatographed on a silica column with CH2Cl2:MeOH (9:1 (v/v)) as eluent. Collection of the fractions containing pure product and evaporation of the solvent afforded pure amine (15 mg, 71%); MS m/z (relative intensity, 70 eV) 295 (M+, 1), 280 (7), 266 (bp), 187 (4), 129 (4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE046117E1
Source datasetuspto-grants-2016_08
ORD IDord-557ddb30738b4b74a1ed7c20d0152b41
Source noteuspto-grants-2016_08