HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881373Generated: November 1, 2026
Hydrochloric Acid → HCID 178516577, compound
https://huagongshe.com/reaction/1881373
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178498574 | HCID 178498574 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178516577 | HCID 178516577 | 77% |
Reaction Steps
To the intermediate (400 mg, 0.77 mmol) was added degassed 2N—NaOH (0.7 mL, 0.35 mmol) and the reaction mixture was stirred at 110° C. for 2 h. After cooled down to room temperature, the reaction mixture was acidified with 1N—HCl. The white precipitate was filtered and dried to give 5-(4,6-Bis-methoxymethoxy-biphenyl-3-yl)-4-naphthalen-1-yl-4H-[1,2,4]triazole-3-thiol as a white solid (250 mg, 65%). 5-(4,6-Bis-methoxymethoxy-biphenyl-3-yl)-4-naphthalen-1-yl-4H-[1,2,4]triazole-3-thiol (190 mg, 0.38 mmol) was dissolved in MeOH (7 mL) and 6N—HCl (0.5 mL) was added to the solution. The reaction mixture was heated at 50° C. for 2 h. After MeOH was removed under vacuum, the reaction mixture was extracted with EtOAc (20 mL×3). The combined organic layers were washed with water and brine and dried over MgSO4. The purification of the concentrated crude product by column chromatography (MeOH 10% in CH2Cl2) afforded the title product as white solid (120 mg, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318790B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-5a5eaeae83c944fe9ba8b248de8f7bc1 |
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| Source note | uspto-grants-2012_11 |
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