HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286592Generated: October 31, 2026
Ethyl chloroformate → HCID 15572311, compound
https://huagongshe.com/reaction/2286592
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15572247 | HCID 15572247 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15572311 | HCID 15572311 | — |
Reaction Steps
A mixture of 700 mg. (2 mmoles) of 4,5-bis(4-fluorophenyl)-2-(trifluoromethylthio)pyrrole and 330 mg. (3 mmoles) of potassium tert-butoxide in 20 ml. of toluene was heated to reflux with stirring and then cooled to room temperature under nitrogen. A solution of 700 mg. (6 mmoles) of ethyl chloroformate in 15 ml. of toluene was then added dropwise and the reaction mixture stirred at room temperature for several hours. The mixture was poured onto an aqueous sodium bicarbonate solution and the product extracted into methylene chloride. The combined organic layers were dried and concentrated to give 800 mg. of a viscous oil. The oil was purified by chromatography on Silic AR CC-7 (eluted by hexane and then by mixtures of hexane/toluene), followed by recrystallization from ethanol/water to give 400 mg. of product as colorless crystals, m.p. 54°-54.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04267184 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-10e12214f6e147fb805381c0adbd254c |
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| Source note | uspto-grants-1981_05 |
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