HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326512Generated: October 26, 2026
Acetic Acid → 4-{2-(4-Hexylphenyl)thiazole-5-yl}phenol
https://huagongshe.com/reaction/326512
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2-(4-Hexylphenyl)-5-(4-methoxyphenyl)-1,3-thiazole | HCID 21997164 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-{2-(4-Hexylphenyl)thiazole-5-yl}phenol | HCID 23354762 | 75.8% |
Reaction Steps
Then, in a 300 ml-three-necked flask, 13.9 g (39.3 mM) of 2-(4-hexylphenyl)-5-(4-methoxyphenyl)thiazole, 76.5 ml of acetic acid and 69.5 ml of 47%-hydrobromic acid were placed, followed by heat-stirring for 16 hours at 100°-110° C. After the reaction, the reaction mixture was poured into cool water, followed by extraction with ethyl acetate. The organic layer was successively washed with water, 5%-sodium hydrogencarbonate aqueous solution and water, followed by distilling-off of the solvent under reduced pressure. The residue was dissolved in a mixture solvent of ethanol/chloroform=1/1, followed by decolorization with activated carbon and distilling-off of the solvent under reduced pressure. The resultant residue was recrystallized two times from toluene to obtain 10.0 g of 2-(4-hexylphenyl)-5-(4-hydroxyphenyl)thiazole (Yield: 75.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05269964 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-c0b17505d4d044d4bd5243b7bb2330f2 |
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| Source note | uspto-grants-1993_12 |
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