HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56465Generated: October 29, 2026
Sodium borohydride → 5-(1,3-Dioxolan-2-yl)-2-fluoro-3',5'-dimethoxybiphenyl-4-amine
https://huagongshe.com/reaction/56465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(6-Fluoro-3',5'-dimethoxy-4-nitrobiphenyl-3-yl)-1,3-dioxolane | HCID 118036540 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 5-(1,3-Dioxolan-2-yl)-2-fluoro-3',5'-dimethoxybiphenyl-4-amine | HCID 118036124 | 88% |
Reaction Steps
A mixture of 2-(6-fluoro-3′,5′-dimethoxy-4-nitrobiphenyl-3-yl)-1,3-dioxolane (1.8 g, 5.2 mmol), sodium borohydride (587.9 mg, 15.5 mmol) and 10% palladium on carbon (0.2 g) in ethanol/water (33 mL, v/v=10/1) was heated at 90° C. for 1 hour. After that, the mixture was diluted with ethyl acetate (150 mL), and washed by water (50 mL) and brine (50 mL). The organic layer was dried over sodium, filtered and concentrated. The residue was purified by silica gel column chromatography (petroleum ether/ethyl acetate=5/1 to 4/1) to afford the title compound (1.4 g, 88%) as a yellow solid. MS (ES+) C17H18FNO4 requires: 319, found: 320 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434700B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-79dcf193974c411b9a5ca8d872515215 |
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| Source note | uspto-grants-2016_09 |
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