HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937162Generated: October 31, 2026
Sodium Bicarbonate → HCID 178462434, compound
https://huagongshe.com/reaction/1937162
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | (2R,3R)-2-(2,4-difluorophenyl)-3-[[1-(hydroxymethyl)-2-hydroxyethyl]-thio]-1-(1H-1,2,4-triazol-1-yl)-2-butanol | HCID 10594623 | — |
| Reactant | 4-[(1E,3E)-5-Oxo-1,3-pentadien-1-yl]benzonitrile | HCID 10655053 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178462434 | HCID 178462434 | 81.3% |
Reaction Steps
A mixture of 240 mg (1.31 mmol) of 4-[(1E,3E)-5-oxo-1,3-pentadienyl]benzonitrile [prepared as described in Step 1(i) above], 392 mg (1.09 mmol) of (2R,3 R)-2-(2,4-difluorophenyl)-3-[[1-(hydroxymethyl)-2-hydroxyethyl]thio]-1-(1H-1,2,4-triazol-1-yl)-2-butanol [prepared as described in Japanese Patent Application (Kokai) Hei 8-333350)], 249 mg (1.31 mmol) of p-toluenesulfonic acid monohydrate, 16 ml of dichloromethane and 3.9 a of molecular sieves 4A was stirred at ambient temperature over night. Aqueous sodium hydrogen carbonate was then added to the reaction mixture and insoluble material was removed by filtration. The resulting filtrate was extracted with ethyl acetate and the organic layer was dried and then concentrated. The resulting residue was purified by chromatography on silica Gel (15 g) column using a 1:1 mixture of ethyl acetate and hexane as the eluant to give 465 mg (yield 81%) of the title compound as a solid. This solid was recrystallized from a mixture of ethyl acetate and hexane to afford crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06392082B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-814ea813070b4c65a2eb21996f0efb31 |
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| Source note | uspto-grants-2002_05 |
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