HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626422Generated: October 30, 2026
Triethylamine → Ethyl (3R)-N-[(benzyloxy)carbonyl]-4,4,4-trifluorovalinate
https://huagongshe.com/reaction/626422
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | Ethyl (3R)-4,4,4-trifluorovalinate | HCID 124507558 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl (3R)-N-[(benzyloxy)carbonyl]-4,4,4-trifluorovalinate | HCID 131735215 | — |
Reaction Steps
23.5 g of ethyl (3R)-4,4,4-trifluorovalinate (diastereomer mixture, crude product about 70%) and 18.1 ml (130 mmol) of triethylamine were dissolved in 235 ml of THF, and 32.3 g (130 mmol) of N-(benzyloxycarbonyloxy)succinimide were added. The reaction mixture was stirred at RT overnight and then diluted with ethyl acetate. The mixture was washed successively with sat. sodium bicarbonate solution, 1 N hydrochloric acid and sat. sodium chloride solution. The organic phase was dried over magnesium sulphate and concentrated under reduced pressure. The crude product was purified by chromatography on silica gel (mobile phase cyclohexane/ethyl acetate 6:1). This gave 22.1 g of the target product (about 80% 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-644dfd2ddfac4395b34d51c7104b1398 |
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| Source note | uspto-grants-2016_04 |
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