HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262444Generated: November 1, 2026
Triethylamine → Isopropyl (2Z)-3-hydroxy-2-cyano-4-ethyl-2-hexenoate
https://huagongshe.com/reaction/2262444
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isopropyl cyanoacetate | HCID 25917 | — |
| Reactant | 2-Ethylbutyryl chloride | HCID 75954 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isopropyl (2Z)-3-hydroxy-2-cyano-4-ethyl-2-hexenoate | HCID 54693160 | 68% |
Reaction Steps
22.2 g (0.16 mol) of 2-ethylbutyryl chloride were added to a solution of 21 g (0.16 mol) of isopropyl cyanoacetate in CH2Cl2, and the reaction mixture was cooled to 0° C. At this temperature, with ice-cooling, 33.5 g (0.33 mol) of triethylamine were added dropwise, and the mixture was then stirred at 25° C. for 2 h. Following subsequent acidic hydrolysis, the organic phase was washed, dried and concentrated. Purification by customary methods gave 24.4 g of the title compound (68% of theory) as a colorless oil (b.p. 70-75° C./1.5 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851411B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-461234f4e4274a74b54408507a4eb786 |
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| Source note | uspto-grants-2010_12 |
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