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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277272Generated: October 31, 2026

Tetrahydrofuran → HCID 86731351, compound

https://huagongshe.com/reaction/2277272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86731349HCID 86731349—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 86731351HCID 8673135163.3%

Reaction Steps

To a mixture of N-((2S)-1-((2-(3-acetyl-4-ethoxy-5-fluorophenyl)-1,3-benzoxazol-6-yl)oxy)propan-2-yl)acetamide (660 mg), THF (10 mL) and methanol (5 mL) was added sodium borohydride (60.3 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 diluted with ethyl acetate, and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate-ethyl acetate/methanol) to give the title compound (420 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-e3114e8ac6c64316b4c6b9efd1357331
Source noteuspto-grants-2015_09