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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474495Generated: October 30, 2026

HCID 86689435, compound → HCID 86689434, compound

https://huagongshe.com/reaction/1474495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86689435HCID 86689435—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86689434HCID 86689434—

Reaction Steps

To a solution of 90.0% 2-(4-iodophenyl)-7-((tetrahydro-2H-pyran-2-yl)oxy)-3-(4-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)chroman-4-one (104.891 g, 150.7 mmol, 1.0 equiv.) in THF (1.2 L) at 5° C., was added Methylmagnesium chloride 3.0 M solution in THF (160.000 ml, 480.0 mmol, 3.2 equiv.) by addition funnel over 30 minutes. The temperature did not rise about 8° C. during the addition. The reaction was removed from the ice bath and stirred at room temperature and stirred for another hour. TLC (20% ethyl acetate in hexanes) showed the reaction had no starting material. The solution was cooled in an ice bath, and carefully quenched with saturated ammonium chloride (35 mL). Ethyl acetate (1.2 L) and water (1.2 L) were added to the reaction mixture, and the layers were separated. The aqueous layer was extracted with EA (1 L). The combined organic layer was washed with brine (1 L), dried over anhydrous Na2SO4, filtered and concentrated in vacuo to yield a pale yellow foam (111.26 g crude). This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018244B2
Source datasetuspto-grants-2015_04
ORD IDord-c5dfe5cec87748838f2f0520998e8bf3
Source noteuspto-grants-2015_04