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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915570Generated: October 31, 2026

Tetrahydrofuran → HCID 86630678, compound

https://huagongshe.com/reaction/1915570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86630675HCID 86630675—
CatalystTetraethylammonium ChlorideHCID 5946—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86630678HCID 86630678—

Reaction Steps

400 mg 4-(3-bromo-6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde (prepared as described under example 31), 504 mg tributyl(vinyl)stanane, 176 mg tetraethylammonium chloride, 147 mg K2CO3 and 19 mg Pd(PPh3)2Cl2 are suspended in 10 ml THF under a nitrogen atmosphere. The mixture is heated (microwave irradiation) to 110° C. for 45 min. This mixture is worked up by diluting with water and extraction with dichloromethane. The combined organic layers are dried over Na2SO4 and concentrated to yield the crude product, which is purified by chromatography on silica gel (ethyl acetate/dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614218B2
Source datasetuspto-grants-2013_12
ORD IDord-9fa5f70713fe4055923d0a29d4a82c09
Source noteuspto-grants-2013_12