HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247513Generated: October 30, 2026
3-Fluorobenzylamine → HCID 66960456, compound
https://huagongshe.com/reaction/2247513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluorobenzylamine | HCID 66853 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Reactant | HCID 86602477 | HCID 86602477 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66960456 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687640B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-2fee08e6a0b44db489c2b1401c535841 |
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| Source note | uspto-grants-2010_03 |
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