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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl succinimido carbonateHCID 83172—
ReactantEthyl (3R)-4,4,4-trifluorovalinateHCID 124507558—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl (3R)-N-[(benzyloxy)carbonyl]-4,4,4-trifluorovalinateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309198B2
Source datasetuspto-grants-2016_04
ORD IDord-644dfd2ddfac4395b34d51c7104b1398
Source noteuspto-grants-2016_04