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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798048Generated: November 2, 2026

Hydrochloric Acid → HCID 58292615, compound

https://huagongshe.com/reaction/1798048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 67252001HCID 67252001—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58292615HCID 5829261570.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl-2-(4-fluoro-1-hydroxy-6-(tetrahydro-2H-pyran-2-yloxy)-1,3-dihydro benzo[c][1,2]oxaborol-3-yl)acetate (0.34 g, 1.0 mmol) in THF (10 mL) was added dropwise concentrated hydrochloride acid (0.2 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 h and quenched by addition of sat. aqueous NaHCO3 (20 mL). The resulting mixture was extracted with EtOAc(2×30 mL). The combined extracts were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica gel (EtOAc/PE=1/4) to give the title compound as a light yellow solid (180 mg, Yield: 70.9%). 1H NMR (400 MHz, DMSO-d) δ 9.93 (s, 1H), 9.40 (s, 1H), 6.94-6.94 (d, J=1.6 Hz, 1H), 6.65-6.68 (m, 1H), 5.49-5.52 (m, 1H), 4.00-4.08 (m, 2H), 2.94-2.99 (m, 1H), 2.38-2.44 (m, 1H), 1.13-1.20 (m, 3H). MS (ESI) m/z=255 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343944B2
Source datasetuspto-grants-2013_01
ORD IDord-1019a338f9ab417ab0e58c22cd4b5519
Source noteuspto-grants-2013_01