HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626424Generated: October 31, 2026
Triethylamine → Ethyl (3R)-N-[(allyloxy)carbonyl]-4,4,4-trifluorovalinate
https://huagongshe.com/reaction/626424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | Ethyl (3R)-4,4,4-trifluorovalinate | HCID 124507558 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl (3R)-N-[(allyloxy)carbonyl]-4,4,4-trifluorovalinate | HCID 131735216 | — |
Reaction Steps
9.7 ml (69.3 mmol) of triethylamine were added dropwise to a solution of 6.38 g (55.4 mmol) of succinimide in 90 ml of abs. THF. The resulting suspension was cooled to 0° C., and a solution of 6.68 g (55.4 mmol) of allyl chloroformate in 10 ml of abs. THF was added dropwise. The mixture was stirred at 0° C. for 1 h, and three portions of in total 9.2 g (about 46 mmol) of ethyl (3R)-4,4,4-trifluorovalinate (diastereomer mixture, crude product) were added. The reaction mixture was warmed to RT overnight, then diluted with ethyl acetate, washed with sat. sodium bicarbonate solution and sat. sodium chloride solution, dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by chromatography on silica gel (mobile phase cyclohexane/ethyl acetate 10:1→4:1). This gave 6.50 g of the target product (about 50% of theory, diastereomer ratio about 2:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309198B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-3fe86a5cfd3b4932aa9e84601ab655f1 |
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| Source note | uspto-grants-2016_04 |
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