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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSuccinimideHCID 11439—
ReactantAllyl chloroformateHCID 18052—
ReactantEthyl (3R)-4,4,4-trifluorovalinateHCID 124507558—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl (3R)-N-[(allyloxy)carbonyl]-4,4,4-trifluorovalinateHCID 131735216—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309198B2
Source datasetuspto-grants-2016_04
ORD IDord-3fe86a5cfd3b4932aa9e84601ab655f1
Source noteuspto-grants-2016_04