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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670643Generated: October 29, 2026

Triphenylphosphine → HCID 57748742, compound

https://huagongshe.com/reaction/1670643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 57748785HCID 57748785—
ReactantHCID 67335785HCID 67335785—
Catalystpalladium(II) acetateHCID 167845—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 57748742HCID 5774874289.9%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994164B2
Source datasetuspto-grants-2011_08
ORD IDord-d24a4b987e6d4ffcad5b8557338b2fd0
Source noteuspto-grants-2011_08