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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937155Generated: October 31, 2026

p-Toluenesulfonic acid monohydrate → HCID 178462431, compound

https://huagongshe.com/reaction/1937155

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-Fluoro-4-[(1E,3E)-5-oxo-1,3-pentadienyl]benzonitrileHCID 10219852—
Reactant(2R,3R)-2-(2,3-difluorophenyl)-3-[[1-(hydroxymethyl)-2-hydroxyethyl]thio]-1-(1H-1,2,4-triazol-1-yl)-2-butanolHCID 69943646—
ProductHCID 178462431HCID 17846243155%

Reaction Steps

Crude title compound was obtained as an oil in a similar manner to that described in Example 1(iii) above using 643.3 mg (1.80 mmol) of (2R,3R)-2-(2,3-difluorophenyl)-3-[[1-(hydroxymethyl)-2-hydroxyethyl]thio]-1-(1H-1,2,4-triazol-1-yl)-2-butanol [prepared as described in Step 7(vi) above], 361.8 mg (1.80 mmol) of 3-fluoro-4-[(1E,3E)-5-oxo-1,3-pentadienyl]-benzonitrile [prepared as described in Example 1(ii) above] and 376.3 mg (1.98 mmol) of p-toluenesulfonic acid monohydrate. The oil was purified by chromatography on a silica gel (50 g) column using a 1:1 mixture of ethyl acetate and hexane as the eluant to give 533.7 mg (yield 55%) of the title compound as a colorless non-crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06392082B1
Source datasetuspto-grants-2002_05
ORD IDord-c6c9b2e2a8ba4c25bffa5f76e5d75136
Source noteuspto-grants-2002_05