HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670643Generated: October 29, 2026
Triphenylphosphine → HCID 57748742, compound
https://huagongshe.com/reaction/1670643
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 57748785 | HCID 57748785 | — |
| Reactant | HCID 67335785 | HCID 67335785 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 57748742 | HCID 57748742 | 89.9% |
Reaction Steps
Degas three times a mixture of (4-bromo-2-nitro-phenyl)-((7S,8aS)-hexahydro-pyrrolo[2,1-c][1,4]oxazin-7-yl)-amine (0.011 mol, 4.0 g), (E)-3,7-difluoro-11-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-ylmethylene)-6,11-dihydro-dibenzo[b,e]oxepine (0.012 mol, 4.76 g), triphenylphosphine (0.0031 mol, 0.8 g) and sodium methoxide (0.03 mol, 1.6 g) in tetrahydrofuran/methanol (3:1) (120 mL) with nitrogen. Add palladium (II) acetate (1.0 mmol, 240 mg) to the reaction mixture and degas again three times with nitrogen. Heat the reaction mixture at 70° C. for 4 h. Cool the reaction mixture to room temperature, filter through a plug of diatomaceous earth and concentrate the filtrate under reduced pressure to obtain the title compound (5.0 g, crude).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994164B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-d24a4b987e6d4ffcad5b8557338b2fd0 |
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| Source note | uspto-grants-2011_08 |
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