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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836462Generated: October 27, 2026

Sodium cyanoborohydride → Benzenemethanamine, 4-fluoro-N-methoxy-

https://huagongshe.com/reaction/1836462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-Fluoro-benzaldehyde O-methyl-oximeHCID 53963238—
SolventAcetic AcidHCID 176—
ProductBenzenemethanamine, 4-fluoro-N-methoxy-HCID 1214706075%

Reaction Conditions

Temperature25 °C

Reaction Steps

In an alternative procedure a solution of 4-fluorobenzaldehyde O-methyloxime (0.82 g, 5.35 mmol) in acetic acid ( 8 ml ) was treated at 10° C. with sodium cyanoborohydride (0.67 g, 10.7 mmol) added in small portions over 10 min and the resulting solution was stirred at 25° C. for 18 h. The solvent was evaporated under reduced pressure (co-evaporation with toluene twice) and the residue was slurried with water and the pH was adjusted to 9 with 2 N aqueous sodium hydroxide. The aqueous phase was extracted twice with ether 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 hexane-ethyl acetate, 8:2) and distilled in vacuo to give 0.62 g (75% yield) of the title amine as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777440B2
Source datasetuspto-grants-2004_08
ORD IDord-9566c8a0c167463ea3cc97075fef2179
Source noteuspto-grants-2004_08