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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480434Generated: November 1, 2026

Formaldehyde → tert-Butyl 4-[2-(methylamino)ethyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1480434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactanttert-Butyl 4-(2-aminoethyl)piperidine-1-carboxylateHCID 1514258—
ReactantSodium triacetoxyborohydrideHCID 5049666—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-[2-(methylamino)ethyl]piperidine-1-carboxylateHCID 46835695—

Reaction Steps

Tert-butyl 4-(2-aminoethyl)piperidine-1-carboxylate (1.0 g, 4.38 mmol) was dissolved in DCM (40 ml) and treated with 36.5% formaldehyde solution (326 μl, 4.38 mmol) followed by acetic acid (1 drop). The reaction mixture was stirred for 20 mins and treated with sodium triacetoxyborohydride (93 mg, 0.438 mmol). The resulting mixture was stirred at ambient temperature for 16 hrs and quenched with 2M NaOH (40 ml). The mixture was extracted with DCM (2×100 ml) and the combined organic extracts were dried (MgSO4) and concentrated under reduced pressure to give tert-butyl 4-(2-(methylamino)ethyl)piperidine-1-carboxylate as an oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409895B2
Source datasetuspto-grants-2016_08
ORD IDord-e445386113dd44bb933994f9f910d2da
Source noteuspto-grants-2016_08