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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246928Generated: October 30, 2026

Water → HCID 20598048, compound

https://huagongshe.com/reaction/1246928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 54543759HCID 54543759—
SolventSodium BicarbonateHCID 516892—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductHCID 20598048HCID 20598048—

Reaction Conditions

Temperature70 °C

Reaction Steps

3(R)-(Phenyl-propionyl-amino)-piperidine-1-carboxylic acid tert-butyl ester (169) (100 mg) was dissolved in a mixture of TFA-CH2Cl2 (1 ml, 20%) and stirred for 1 hr. After removal of solvent, the residue was dried under vacuum for 30 min and dissolved in 5 ml of CH2Cl2, washed with sat. K2CO3, dried (Na2SO4), filtered. After evaporation of the solvent, the residue was dissolved in CH3CN (1 ml). Then K2CO3 (125 mg, 3 eq), water (1 ml) and (2-bromoethyl)benzene (0.05 ml, 1.2 eq) was added. The mixture was heated at 70° C. for 12 hr. After cooling to room temperature, the mixture was diluted with sat. NaHCO3 (5 ml), extracted with CH2Cl2 (2×10 ml). The combined organic layers were dried (Na2SO4), filtered and evaporated. The residue was purified by silica gel chromatography (100% CH2Cl2, 2%–4% MeOH in CH2Cl2) to give 170 as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129228B2
Source datasetuspto-grants-2006_10
ORD IDord-4bfc1459ee294844bb2e8c3e9ec0fb3b
Source noteuspto-grants-2006_10