Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091657Generated: November 2, 2026

Formaldehyde → HCID 66593552, compound

https://huagongshe.com/reaction/1091657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 66593311HCID 66593311—
SolventMethanolHCID 887—
ProductHCID 66593552HCID 6659355298.7%

Reaction Steps

(R)—N-(4-Amino-3-nitrophenyl)piperidine-2-carboxamide (2.09 g, 7.9 mmol) was dissolved in MeOH (50 mL), and paraformaldehyde (0.95 g) and sodium cyanoborohydride (0.50 g, 8.0 mmol) were added. The mixture was stirred at room temperature for 70 min, and water added dropwise. The solvent was evaporated and the residue partitioned between water and EA (150 mL each). The phases were separated and the aqueous phase extracted with EA (2×100 mL). The combined EA layers were washed with brine, dried over magnesium sulfate, and concentrated to give (R)—N-(4-amino-3-nitrophenyl)-1-methylpiperidine-2-carboxamide as an orange foam (2.17 g), which was used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129396B2
Source datasetuspto-grants-2012_03
ORD IDord-eb383c9d4db84b11b6527481fc2087c3
Source noteuspto-grants-2012_03