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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053514Generated: November 3, 2026

Thiophenol → HCID 131736280, compound

https://huagongshe.com/reaction/1053514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantDabcoHCID 9237—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 10560973HCID 10560973—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131736280HCID 13173628085.9%

Reaction Steps

To a stirred solution of 1,4-diazabicyclo[2.2.2]octane (DABCO, 10 mg, 0.89 mmol) and thiophenol (99 mg, 0.89 mmol) in dry THF (20 mL) at RT was added compound 1 (200 mg, 0.89) dissolved in dry THF (2 mL) through a syringe over 12 min. The reaction mixture was further stirred for 20 min. 10% NaOH(aq) was added. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and the solvent was removed by evaporation. The crude product was purified by column chromatography using ethyl acetate:hexane (2:8) as an eluent to give compound 4 (254 mg, 85%). 1H NMR (400 MHz, CDCl3) δ 5.84 (d, J=15.0 Hz, 1H), 7.18 (d, J=8.6 Hz, 2H), 7.46 (m, 6H), 7.58 (m, 6H), 8.05 (d, J=15.0 Hz, 1H). HRMS ESI (m/z): Calculated for C21H16O2S ([M+H]+): 333.0871. found: 333.0852.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393306B2
Source datasetuspto-grants-2016_07
ORD IDord-8a43e9d4c685497e96d97330ced86ffe
Source noteuspto-grants-2016_07