HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421967Generated: October 30, 2026
Water → 2-(3,4-Diethoxyphenyl)-4-styrylthiazole
https://huagongshe.com/reaction/1421967
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(3,4-Diethoxyphenyl)-4-formylthiazole | HCID 18707207 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Benzyltriphenylphosphonium chloride | HCID 70671 | — |
| Product | 2-(3,4-Diethoxyphenyl)-4-styrylthiazole | HCID 53991872 | — |
Reaction Steps
4.2 ml of n-butyllithium was dropwise added in small portions to a suspension of 2.6 g of benzyltriphenylphosphonium chloride in 10 ml of tetrahydrofuran, with stirring at -50° C. The mixture was heated to room temperature and, after cooling again to -50° C., was mixed with 12 ml of a tetrahydrofuran solution of 2 g of 2-(3,4-diethoxyphenyl)-4-formylthiazole. The mixture was stirred at the same temperature for 30 minutes and at room temperature for 14 hours. 10 ml of water and 40 ml of ethyl acetate were added to conduct extraction and phase separation. The solvent layer was dried and subjected to distillation to remove the solvent. The residue was purified by silica gel column chromatography to obtain 2 g of 2-(3,4-diethoxyphenyl)-4-styrylthiazole as a 1:1 mixture of cis form and trans form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06080764 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-0ffe3ef37b0d469b8ae44a2348190dfb |
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| Source note | uspto-grants-2000_06 |
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