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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517773Generated: October 25, 2026

Formaldehyde → HCID 86691894, compound

https://huagongshe.com/reaction/517773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantAzidotrimethylsilaneHCID 78378—
Reactant(R)-3-MethylmorpholineHCID 641498—
ReactantHCID 25192390HCID 25192390—
SolventMethanolHCID 887—
ProductHCID 86691894HCID 86691894—

Reaction Steps

To a solution of (3R)-3-methylmorpholine (51.6 mg, 0.510 mmol, Tyger Scientific, Ewing, USA) in methanol (2 mL) was added formaldehyde (37% aqueous) (0.038 mL, 0.510 mmol). The reaction mixture was stirred at room temperature for 1 hour before the addition of 4-isocyano-2-(trifluoromethyl)benzonitrile (100 mg, 0.510 mmol, commercially available from Priaxon AG, Munich, Germany) and trimethylsilylazide (0.068 mL, 0.510 mmol). The reaction mixture was stirred at room temperature overnight (approximately 18 hours) and the solvent removed under vacuum. The residue was purified by MDAP. Fractions containing the desired compound were combined and the solvent removed. The residue was partitioned between saturated NaHCO3 (2 mL) and DCM (5 ml). The organic layer was collected via a hydrophobic frit and the solvent removed under a stream of argon. The compound was dissolved in a minimum of diethyl ether before the addition of 1N HCl in diethyl ether (2 mL) leading to precipitation. The ether was removed under vacuum and the product further dried under vacuum at 40° C. overnight to yield the title compound as a white solid (57 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115132B2
Source datasetuspto-grants-2015_08
ORD IDord-7553ba9e09ab4a698a9f520f206438f6
Source noteuspto-grants-2015_08