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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356643Generated: October 25, 2026

1,5-Dibromopentane → (R)-2-Piperidino-2-phenylethanol

https://huagongshe.com/reaction/356643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DibromopentaneHCID 8100—
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-beta-aminophenethyl alcoholHCID 2724025—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product(R)-2-Piperidino-2-phenylethanolHCID 11333205138.3%

Reaction Steps

A suspension mixture of (R)-(-)-2-phenylglycinol(686 mg, 5 mmol), 1,5-dibromopentane (0.82 ml, 6 mmol), and K2CO3 (1.38 g, 10 mmol) in ethanol (15 ml) was refluxed with stirring for 23 h. After cooling down to rt, the white solid was removed by filtration and the filtrate was concentrated to give white solid oil mixture. This was suspended in CH2Cl2 (30 ml), washed with water and saturated NaHCO3 aqueous solution, dried (Na2SO4), and concentrated to give 1.42 g of clear yellow oil. This was purified by column chromatography (silica gel: 50 g, CH2Cl1 /MeOH:30/1 to 20/1) to afford 955 mg (93%) of desired compound as clear light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837717
Source datasetuspto-grants-1998_11
ORD IDord-22206538a3d8469da3f1db0fed58bfb5
Source noteuspto-grants-1998_11