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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889664Generated: October 25, 2026

Dichloromethane → tert-Butyl 4-((4-fluorobenzylamino)methyl)benzylcarbamate

https://huagongshe.com/reaction/1889664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactanttert-butyl N-{[4-(aminomethyl)phenyl]methyl}carbamateHCID 3354775—
ReactantSodium borohydrideHCID 4311764—
SolventIsopropanolHCID 3776—
Producttert-Butyl 4-((4-fluorobenzylamino)methyl)benzylcarbamateHCID 6661676250.1%

Reaction Steps

To a solution of 4-fluorobenzaldehyde (496 mg, 4.00 mmol) in a mixed solvent of CH2Cl2 (10 mL) and 2-propanol (2 mL) at rt was added tert-butyl 4-(aminomethyl)benzylcarbamate (945 mg, 4.00 mmol, Aldrich). The reaction mixture was stirred at rt overnight. The next morning, sodium borohydride (296 mg, 8.0 mmol) was added, and the mixture was stirred at rt for 2 h. The reaction mixture was quenched by adding 3 mL of MeOH and 3 mL of saturated aq NaHCO3. The mixture was extracted with EtOAc (3×50 mL). The combined organic extracts were dried, concentrated and purified by flash column chromatography on silica gel eluting with CH2Cl2/EtOAc to give the title compound (0.69 g, 48%) as a viscous material. MS (ESI): 345.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-2e54c2e4e57942c2af608bf31b6a189f
Source noteuspto-grants-2013_08