HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090726Generated: November 1, 2026
Ethyl chloroformate → HCID 15023300, compound
https://huagongshe.com/reaction/1090726
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 15023251 | HCID 15023251 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15023300 | HCID 15023300 | 37.6% |
Reaction Steps
Into 20 ml of anhydrous ether was dissolved 4.00 g (15 mmol) of 2-tetradecylpyrrole obtained in Synthetic Example 2, and then 7 ml (21 mmol) of ca. 3M ethereal solution of methylmagnesium bromide was added thereto at room temerature. The resulting mixture was heated under reflux for 30 minutes. Under cooling with ice water, 2 ml (21 mmol) of ethyl chlorocarbonate was added to the mixture. After heating under reflux for 10 hours, the resulting mixture was cooled to room temperature, poured into ice water containing ammonium chloride, and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous megnesium sulfate. After removing the solvent under reduced pressure, the residue was purified by subjecting it to column chromatography (eluent: ethyl acetate/hexane=1/10) to obtain 1.89 g (37% yield) of ethyl 5-tetradecylpyrrole-2-carboxylate, m.p. 60°-63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05082856 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-6982d665f45b490d9e9375228e071cdc |
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| Source note | uspto-grants-1992_01 |
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