HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564436Generated: October 30, 2026
Water → [5'-(Aminomethyl)-2'-fluoro-3-biphenylyl]methanol
https://huagongshe.com/reaction/564436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Bromo-4-fluorophenyl)methanamine hydrochloride | HCID 2724901 | — |
| Reactant | [3-(Hydroxymethyl)phenyl]boronic acid | HCID 2734662 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | [5'-(Aminomethyl)-2'-fluoro-3-biphenylyl]methanol | HCID 57813296 | 13.2% |
Reaction Steps
To a solution of [3-(hydroxymethyl)phenyl]boronic acid (2 g, 13.2 mmol) in 1,4-dioxan (40 mL) was added [(3-bromo-4-fluorophenyl)methyl]amine hydrochloride (3.18 g, 13.2 mmol), potassium carbonate (9.1 g, 66 mmol) and tetrakis(triphenylphosphine)-palladium(0) (456 mg, 0.4 mmol). The mixture was split into 4×20 mL capacity microwave vials and each was treated with water (3 mL). The mixtures were each heated at 150° C. for 20 min. One sixth of the total reaction mixture was treated with water (100 mL) and extracted with ethyl acetate (2×80 mL). The combined organic phase was dried (magnesium sulphate) and concentrated to dryness and the product purified by flash chromatography on silica using 0-50% ethyl acetate/cyclohexane followed by dichloromethane/ammonia solution/methanol @ 8:1:1 as eluants. Product-containing fractions were combined and concentrated to dryness to afford 402 mg of the title compound. LC-MS m/z 463 (M+H)+, 0.65 min (ret time). The remaining five-sixth of the reaction mixture was worked up in the same manner and purified by flash chromatography using ethyl acetate/cyclohexane @ 1:1 followed by dichloromethane/ammonia solution/methanol @ 8:1:1 as eluants. This yielded 1.97 g of the title compound. LC-MS m/z 463 (M+H)+, 0.65 min (ret time).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067408B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-c46e0a2bb08740f184c970e86a1e0d7d |
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| Source note | uspto-grants-2011_11 |
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