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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247513Generated: October 30, 2026

3-Fluorobenzylamine → HCID 66960456, compound

https://huagongshe.com/reaction/2247513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzylamineHCID 66853—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantSodium bicarbonate waterHCID 86585896—
ReactantHCID 86602477HCID 86602477—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66960456HCID 66960456—

Reaction Steps

To a methylene chloride (6 mL) solution of (E)-2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene)-6-oxohexanoic acid ethyl ester (231 mg), 3-fluorobenzylamine (88.7 μL), acetic acid (0.5 mL) and sodium triacetoxy borohydride (165 mg) were added one by one. After agitating the reaction solution at room temperature overnight, a saturated sodium bicarbonate water and ethyl acetate were added to the reaction solution, and the organic layer was partitioned. After the obtained organic layer was washed with a saturated saline solution, it was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (Carrier: Chromatorex NH, elution solvent; heptane-ethyl acetate=1:1->ethyl acetate->ethyl acetate:ethanol=10:1), and 173 mg of the title compound was obtained. The physical properties of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687640B2
Source datasetuspto-grants-2010_03
ORD IDord-2fee08e6a0b44db489c2b1401c535841
Source noteuspto-grants-2010_03