Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279434Generated: November 2, 2026

Formaldehyde → HCID 18770396, compound

https://huagongshe.com/reaction/1279434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 18770462HCID 18770462—
SolventAcetic AcidHCID 176—
SolventAcetonitrileHCID 6342—
ProductHCID 18770396HCID 1877039696.8%

Reaction Steps

A 37% aqueous solution of formaldehyde (5 ml; 67 mmol) and sodium cyanoborohydride (314 mg; 5.0 mmol) were added to a solution in acetonitrile (20 ml) of N,N-bis[(1-tert-butoxycarbonyl-4-piperidinyl)methyl]amine (1.0 g; 2.4 mmol) synthesized by the above process, and the mixture was stirred at room temperature for 15 minutes. Acetic acid was then added to the solution to adjust the pH to about 5, and the mixture was stirred further for 48 hours at room temperature. The reaction mixture was brought to pH about 10 by addition of aqueous 2.5N sodium hydroxide and extracted with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 989 mg (yield: 95%) of N,N-bis[(1-tert-butoxycarbonyl-4-piperidinyl)methyl]-methylamine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448242B1
Source datasetuspto-grants-2002_09
ORD IDord-1b2739fda617434783f8631f85e08a04
Source noteuspto-grants-2002_09