HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 22288406, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 22288390 | HCID 22288390 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Product | HCID 22288406 | HCID 22288406 | — |
Reaction Steps
4-Methyl-3-(2-thienyl)-5-trifluoromethyl-1H-pyrazole was allowed to react with an n-butyl lithium-n-hexane solution (1.6 M). Further, ethyl chloroformate was added at −50° C. or below. After stirring at −50° C. or below for 30 minutes, it was subjected to purification in the usual way to give a yellow oil. By hydrolyzing this in the usual way, 5-(4-methyl-5-trifluoromethyl-1H-pyrazol-3-yl)thiophene-2-carboxylic acid was obtained as colorless powder crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06958339B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-980f33f4969047b5b0ae94d8a686b0e1 |
| Source note | uspto-grants-2005_10 |