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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277215Generated: October 31, 2026

Hydrochloric Acid → HCID 86731281, compound

https://huagongshe.com/reaction/2277215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86731280HCID 86731280—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 86731281HCID 8673128148%

Reaction Conditions

Temperature70 °C

Reaction Steps

To 2-(4-(cyclopropylmethoxy)-3-fluorophenyl)-4,7-dihydro-5H-spiro[1,3-benzoxazole-6,2′-[1,3]dioxolane] (3.75 g) in a mixed solvent of THF (25 mL)-methanol (12.5 mL)-water (12.5 mL) was added 6 M hydrochloric acid (10.8 mL), and the mixture was stirred at 70° C. for 1 hr. The reaction mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. To the organic layer was added sodium tetrahydroborate (411 mg), and the mixture was stirred at room temperature for 20 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 (1.58 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-5cc432b525d44458ad372b6d8a345ee4
Source noteuspto-grants-2015_09