HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358106Generated: October 30, 2026
Trifluoroacetic acid → HCID 20450402, compound
https://huagongshe.com/reaction/358106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 13206728 | HCID 13206728 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20450402 | HCID 20450402 | — |
Reaction Steps
In 5 ml of anhydrous dichloromethane was dissolved 1.146 g of 2-[m-(p-methoxyphenylmethoxycarbonylacetoxy)phenyl]imidazo[2,1-b]benzothiazole and after adding thereto 0.4 ml of anisole, the mixture was cooled with ice-water. Then, 5 ml of trifluoroacetic acid was added dropwise to the mixture and the resultant mixture was stirred for one hour. The reaction mixture thus formed was concentrated under reduced pressure and the oily product thus obtained was dissolved in 10 ml of anhydrous tetrahydrofuran. Then, while stirring the mixture under ice-cooling, 2 ml of 2N hydrogen chloride ethanol solution was added to the solution and white crystals thus precipitated were recovered by filtration to provide 911 mg of 2-(m-carboxyacetoxyphenyl)imidazo[2,1-b]benzothiazole hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04464384 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-a6d31499b13c4a099b7626e686fd8ee8 |
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| Source note | uspto-grants-1984_08 |
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