HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260962Generated: October 30, 2026
Isoamyl Alcohol → HCID 57117418, compound
https://huagongshe.com/reaction/260962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoamyl Alcohol | HCID 31260 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 19436753 | HCID 19436753 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57117418 | HCID 57117418 | 95% |
Reaction Steps
To a solution of 1.9 g (5.0 mmole) of 2-(2-chloro-5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluorophenoxy)-propanoic acid in 50 mL methylene chloride was added 1.3 mL (15.0 mmole) oxalyl chloride over 5 minutes, causing the evolution of gas. When this evolution ceased, one drop of DMF was added and the solution stirred until the gas evolution ceased. The solution was stripped to dryness in vacuo. The acid chloride was dissolved in 40 mL of 3-methyl-1-butanol and heated to reflux for one hour. The reaction mixture was cooled, diluted with 100 mL cold water and extracted with ethyl acetate. The ethyl acetate was washed with brine, dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified chromatographically using 25% ethyl acetate in hexane as the eluent to give 2.17 g (95%) of 2-(2-chloro-5-(4-chloro-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-4-fluorophenoxy)-propanoic acid, 3-methylbutyl ester as a white solid; mp 128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05530126 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-a2c070b0110a4a3da64f0f03d65a5dbf |
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| Source note | uspto-grants-1996_06 |
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