HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656691Generated: October 30, 2026
Ammonium Chloride → Ethyl-2-hydroxy-4-methyl-2-(trifluoromethyl)pentenoate
https://huagongshe.com/reaction/656691
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| Reactant | Ethyl 3,3,3-trifluoro-2-oxopropanoate | HCID 2737239 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl-2-hydroxy-4-methyl-2-(trifluoromethyl)pentenoate | HCID 86624389 | 73% |
Reaction Steps
A suspension of 0.27 mol Mn and 0.01 mol ZnCl2 in 105 ml THF is heated to reflux. 0.01 mol 3-bromo-2-methyl-1-propene is added to the boiling mixture and after 30 minutes a solution of 0.11 mmol ethyl-trifluoropyruvate and 0.18 mol 2-bromo-2-methyl-1-propene in 90 ml THF is dropped to the reaction mixture within 2.5 hours. After 3 hours under reflux the mixture is stirred for 19 hours at room temperature. The reaction mixture is poured on 90 ml of a saturated NH4Cl and ice mixture. After vigorous stirring for 30 minutes the mixture is extracted four times with 110 ml of MTBE each. The combined organic extracts are washed with 30 ml of brine, dried over magnesiumsulfate and concentrated in vacuo. The residue is destined under reduced pressure. ethyl-2-hydroxy-4-methyl-2-(trifluoromethyl)pentenoate is obtained in 73% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071796B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-6db0edf68f1b460596a582f6b8778510 |
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| Source note | uspto-grants-2011_12 |
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