Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500323Generated: November 3, 2026

Acetic Acid → HCID 68408166, compound

https://huagongshe.com/reaction/1500323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-butyl N-methyl-N-(2-oxoethyl)carbamateHCID 10725881—
ReactantHCID 67367332HCID 67367332—
ReactantCID 101953985HCID 101953985—
SolventMethanolHCID 887—
SolventChloroform methanolHCID 21584188—
ProductHCID 68408166HCID 6840816689.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

7 g (1 eq) 4-phenyl-4-(pyrrolidin-1-yl)piperidine bishydrochloride were added to a solution of 4.4 g (1.1 eq) tert-butyl-methyl(2-oxoethyl)carbamate in 70 ml methanol under a nitrogen atmosphere and the reaction mixture was stirred for 10 min at 0° C. 3.62 g (2.5 eq) sodium cyanoboron hydride were then added and the mixture was stirred for 30 min at room temperature. The reaction mixture obtained was adjusted to a pH of 5-6 with acetic acid and stirred for 14 h at room temperature. The reaction course was monitored by thin-layer chromatography (10% MeOH/CHCl3). Once the conversion was complete, the methanol was distilled off, saturated NaHCO3 solution was added and the mixture obtained was extracted with chloroform (3×50 ml) and the combined organic phases were dried over Na2SO4. Following removal of the solvent under reduced pressure, the residue was purified by column chromatography (silica gel; 50% EtOAc/heptane). 8 g (89%) of product were obtained in the form of a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206156B2
Source datasetuspto-grants-2015_12
ORD IDord-a1913d7baf5948c68cae26eed81e746a
Source noteuspto-grants-2015_12