Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387947Generated: October 31, 2026

Sodium cyanoborohydride → HCID 68409171, compound

https://huagongshe.com/reaction/2387947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-butyl N-methyl-N-(2-oxoethyl)carbamateHCID 10725881—
ReactantChloroform methanolHCID 21584188—
ReactantHCID 86633674HCID 86633674—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 68409171HCID 68409171113%

Reaction Steps

A solution of 4.73 g (1 equiv.) of tert-butyl methyl(2-oxoethyl)carbamate in 20 ml of methanol was added at room temperature to a solution of 7 g (1 equiv.) of 4-butyl-N,N-dimethylpiperidine-4-amine bis hydrochloride in 50 ml of methanol, and the resulting reaction mixture was stirred for 50 minutes at room temperature. 3.43 g (2 equiv.) of sodium cyanoborohydride were added in portions to this reaction mixture, and stirring was then carried out for 12 hours at room temperature. The progress of the reaction was monitored by thin-layer chromatography (20% MeOH/CHCl3). When the reaction was complete, the reaction mixture was cooled to 0° C. and adjusted to a pH of ˜5 with acetic acid. 2 g of tert-butyl formylmethyl-methylcarbamate and 1.7 g of sodium cyanoborohydride were then added, and the reaction mixture was stirred for a further 60 minutes at room temperature. Finally, the methanol was distilled off, 100 ml of saturated NaHCO3 solution were added, the resulting mixture was extracted with ethyl acetate (2×200 ml), and the combined organic phases were dried over Na2SO4. After removal of the solvent under reduced pressure, 10.5 g of crude product were obtained in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269000B2
Source datasetuspto-grants-2012_09
ORD IDord-87bbd596026e4e11b09e125ee10c0f93
Source noteuspto-grants-2012_09