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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517385Generated: November 4, 2026

Tetrahydrofuran → HCID 178491755, compound

https://huagongshe.com/reaction/1517385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178491757HCID 178491757—
SolventEthyl AcetateHCID 8857—
ProductHCID 178491755HCID 17849175576%

Reaction Steps

Thionyl chloride (3.22 mmol, 2.5 eq.) was added to a cooled (0° C.) solution of N-((7-(hydroxymethyl)-1H-benzo[d]imidazol-2-yl)methyl)-4-methoxy-N,2,6-trimethylbenzenesulfonamide (1.29 mmol, 1.0 eq.) in abs. THF (10 ml). The reaction mixture was stirred at room temperature for 24 h. The mixture was then diluted with ethyl acetate and washed successively with NaHCO3 solution and NaCl solution. The organic phase was dried over Na2SO4 and the solvent was distilled off in vacuo to obtain the crude product, which led to the desired product by purification by column chromatography over silica gel. Yield: 76%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232288B2
Source datasetuspto-grants-2012_07
ORD IDord-2f150754de9c47cfa1b54ab907a4b0ec
Source noteuspto-grants-2012_07