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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181089Generated: October 27, 2026

Hydrochloric Acid → Benzenemethanamine, 4-fluoro-N-methoxy-

https://huagongshe.com/reaction/2181089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Fluoro-benzaldehyde O-methyl-oximeHCID 53963238—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductBenzenemethanamine, 4-fluoro-N-methoxy-HCID 1214706041%

Reaction Steps

A solution of 4-fluorobenzaldehyde-O-methyloxime (93.2 mmol) in dichloromethane (150 ml) was treated with sodium cyanoborohydride (9.18 g, 0.146 mol) followed by 120 ml of 2 N hydrochloric acid in methanol added dropwise over 30 minutes. After 96 h at 22° C., the solvent was evaporated under reduced pressure, the residue was slurried with water and adjusted to pH 9 with 2 N aqueous sodium hydroxide. The aqueous phase was extracted twice with dichloromethane and the combined organic extracts were washed with brine, dried (magnesium sulfate) and concentrated under reduced pressure. The residual oil was chromatographed on silica gel (elution, toluene-ethyl acetate 0-10%) and gave 5.92 g (41% yield) of the title amine as a clear oil. 1H NMR 400 MHz (CDCl3) δ (ppm): 3.49 (3H, s), 4.01 (2H, s), 5.69 (1H, broad s), 7.01 (2H, m), 7.31 (2H, m). The hydrochloride salt was obtained as a white solid: mp 170-171° C. Anal. calcd for C8H10FNO—HCl: C, 50.14; H, 5.78; N, 7.31. Found: C, 50.31; H, 5.80; N, 7.26

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890942B2
Source datasetuspto-grants-2005_05
ORD IDord-13bd73de2c35454ba938bd4d6d6993f4
Source noteuspto-grants-2005_05