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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121285Generated: November 1, 2026

Hydrochloric Acid → 1-Benzyl-4-(1,3-dihydroxyprop-2-ylamino)-piperidine

https://huagongshe.com/reaction/2121285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantSerinolHCID 68294—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-4-(1,3-dihydroxyprop-2-ylamino)-piperidineHCID 2271204791.5%

Reaction Steps

2.75 g of 2-aminopropan-1,3-diol and 5.9 g of 1-benzyl-4-piperidone are dissolved in 60 ml of methylene chloride and while cooling with ice a total of 9.9 g of sodium triacetoxyborohydride are added batchwise. The mixture is left to stand overnight at ambient temperature. 60 ml of methylene chloride and some water are added, then conc. hydrochloric acid is added while cooling with ice until an acid reaction is obtained. The mixture is stirred for about another 15 min. with cooling and then made clearly alkaline with 4 N sodium hydroxide solution. The aqueous phase is separated off, the organic phase is washed with a very little water, dried over sodium sulphate and freed from solvent in vacuo. 8 g of substance are obtained which are chromatographed with methylene chloride/methanol 8:2 over 150 g of silica gel. The uniform fractions according to TLC are combined and freed from solvent in vacuo. 7.3 g of 1-benzyl-4-(1,3-dihydroxyprop-2-ylamino)-piperidine are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696042B2
Source datasetuspto-grants-2004_02
ORD IDord-23680505e4ef40fba4aaf940d8cac845
Source noteuspto-grants-2004_02