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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277212Generated: November 1, 2026

Ammonium Chloride → HCID 86731276, compound

https://huagongshe.com/reaction/2277212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86731275HCID 86731275—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86731276HCID 86731276—

Reaction Steps

To 2-((2-(4-(cyclopropylmethoxy)-3-fluorophenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-yl)oxy)-1-(morpholin-4-yl)ethanone (4.36 g) in THF (25 mL) was added methylmagnesium bromide (1 M THF solution, 15.2 mL), and the reaction mixture was stirred at room temperature for 10 min. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. To a solution of the obtained residue in a mixed solvent of THF (10 mL)-methanol (10 mL) was added sodium tetrahydroborate (383 mg), and the mixture was stirred at room temperature for 10 min. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (3.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-4f547271244d4d52a5dabd5d8a6310e9
Source noteuspto-grants-2015_09