HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804871Generated: October 30, 2026
Sodium Hydroxide → 2-(4-Methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazole
https://huagongshe.com/reaction/1804871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-(4-Methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazole | HCID 18511698 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazole | HCID 86584258 | 47.1% |
Reaction Steps
To a suspension of 970 mg of 2-(4-methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazole in 30 ml of methanol was added 20 ml of 1,4-dioxane and 5 ml of a 5 N aqueous sodium hydroxide solution. The reaction mixture was refluxed for 3 hours, then concentrated approximately 1/10. Water was added to the residue, and washed with ethyl acetate. To the aqueous layer was acidified with 5 N hydrochloric acid, and extracted with ethyl acetate. The combined organic layer was washed with water and a saturated aqueous sodium chloride solution, and dried with magnesium sulfate. Evaporation the solution, the residue was recrystallized from ethyl acetate to obtain 420 mg of 2-(4-methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazole as a white powder. mp. 191.0-192.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354439B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a1e7d7bc0a544513a9119fb36248199c |
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| Source note | uspto-grants-2013_01 |
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