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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894691Generated: November 3, 2026

Tetrahydrofuran → HCID 19354338, compound

https://huagongshe.com/reaction/1894691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 57867428HCID 57867428—
ReactantHCID 178418573HCID 178418573—
SolventWaterHCID 962—
ProductHCID 19354338HCID 19354338—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of 2-tert-butyl-4H-pyrido[2,3-d][1,3]oxazin-4-one (10.2 g, 50 mmol) and tetrahydrofuran (50 mL) was added methyl magnesium bromide (0.97 m tetrahydrofuran solution, 100 mL, 97 mmol) dropwise at −78° C., after the dropwise addition was finished, which was stirred at −78° C. for 30 minutes. To the reaction mixture were added a saturated aqueous solution of ammonium chloride and water, which was extracted with ethyl acetate, and the organic layer was washed with an aqueous solution of ammonium chloride. The solvent was evaporated under a reduced pressure and the precipitated solid was filtered to obtain the title compound (9.1 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513287B2
Source datasetuspto-grants-2013_08
ORD IDord-661b574e978f40da873a632e2b607f1b
Source noteuspto-grants-2013_08