HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326514Generated: October 31, 2026
Hydrogen Bromide → HCID 15027123, compound
https://huagongshe.com/reaction/326514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | HCID 15027122 | HCID 15027122 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 15027123 | HCID 15027123 | 22.8% |
Reaction Steps
In a 200 ml-round-bottomed flask, 8.20 g (21.6 mM) of 2-(4-octylphenyl)-5-(4-methoxyphenyl)thiazole, 80 ml of a solution of 25%-hydrogen bromide in acetic acid and 3 ml of 57%-hydroiodic acid were placed, followed by heat-stirring for 20 hours at 100° C. After the reaction, the reaction mixture was poured into 200 ml of water, followed by extraction with chloroform. The organic layer was washed with water and dried with anhydrous sodium sulfate, followed by distilling-off of the solvent under reduced pressure. The residue was purified by silica gel column chromatography (eluent: chloroform/ethyl acetate=20/1) to obtain 1.80 g of 2-(4-octylphenyl)-5-(4-hydroxyphenyl)thiazole (Yield: 22.8%).
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-141d787b1f784faa94d2aab60d64b5df |
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| Source note | uspto-grants-1993_12 |
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