HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771812Generated: November 3, 2026
3-(3-Fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-5-methoxy-benzamide → 3-[[3-(3-Fluorophenyl)-5-methoxy-phenyl]methylamino]-2,4-dimethyl-phenol
https://huagongshe.com/reaction/1771812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(3-Fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-5-methoxy-benzamide | HCID 89443728 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[[3-(3-Fluorophenyl)-5-methoxy-phenyl]methylamino]-2,4-dimethyl-phenol | HCID 89443845 | 60.4% |
Reaction Steps
To a solution of 3-(3-fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-5-methoxy-benzamide (1.2 g, 3.3 mmol, 1.0 eq) in THF (50 mL) at 0° C. under N2 was added a solution of BH3 (1M in THF, 16.0 mL, 16.0 mmol, 5.0 eq) dropwise. The reaction mixture was heated at 60° C. overnight then cooled to room temperature and quenched with water. The aqueous layer was extracted with EtOAc and the combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue obtained was purified by column chromatography (petroleum ether:EtOAc, 100:1 to 5:1) to give the title compound as a colorless oil (700 mg, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09249085B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-e03f5d8dec694dfdbe6317d61748e2af |
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| Source note | uspto-grants-2016_02 |
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