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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880586Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 79367550, compound

https://huagongshe.com/reaction/1880586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantTrimethylsulfonium iodideHCID 75127—
Reactant6-Methoxy-1-IndanoneHCID 334036—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 79367550HCID 79367550—

Reaction Conditions

Temperature75 °C

Reaction Steps

A dimethylsulfoxide (8 mL) solution containing sodium hydride (60%, 0.14 g, 3.5 mmol) was heated at 75° C. for ca. 45 minutes. The solution was cooled to room temperature and diluted with THF (8 mL). The solution was cooled to 0° C. and trimethylsulfonium iodide (0.7 g, 3.4 mmol) was added in portions. After 15 minutes a THF solution of 6-methoxyindan-1-one (0.5 g, 3.1 mmol) was added. The solution was then stirred at room temperature for 4 days. The solution was diluted with water and ethyl ether. The organic phase was washed with water (3×) and brine. The solution was then dried over MgSO4, filtered and concentrated. The residue was purified by silica gel chromatography using a hexanes/ethyl acetate gradient to give the title compound. 1H NMR (500 MHz, CDCl3): δ 9.68 (d, J=2.9 Hz, 1H); 7.29 (s, 1H); 7.21 (d, J=8.0 Hz, 1H); 6.86-6.82 (m, 1H); 3.95-3.93 (m, 1H); 3.82 (s, 3H); 3.03-2.93 (m, 2H); 2.48-2.44 (m, 1H); 2.41-2.37 (m, 1H). LCMS1 2.90 min. (M+H)=177

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318760B2
Source datasetuspto-grants-2012_11
ORD IDord-f82a66e2686d44d3a742c6ad471569bb
Source noteuspto-grants-2012_11