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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377640Generated: October 30, 2026

Toluene → Methyl N-{[isopropyl(pent-4-en-1-yl)amino]carbonyl}-3-methyl-L-valinate

https://huagongshe.com/reaction/2377640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantSodium BicarbonateHCID 516892—
ReactantIsopropylpent-4-enylamineHCID 551578—
ReactantMethyl L-tert-leucinate hydrochlorideHCID 16217630—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl N-{[isopropyl(pent-4-en-1-yl)amino]carbonyl}-3-methyl-L-valinateHCID 57692708—

Reaction Steps

To a solution (60 nM) of L-tert-leucine methyl-ester hydrochloride and NaHCO3 (8 eq) in dry THF, a solution 20% w/w of phosgene in toluene (5 eq) was added dropwise at 0° C. and the reaction mixture was stirred at that temperature for 30 minutes. Then the solid was filtered-off and the filtrate evaporated at reduced pressure. The resulting crude yellow oil was taken-up in dry THF (0.3 M) and added dropwise to a stirred solution (0.2 M) of N-isopropylpent-4-en-1-amine and THF (1 eq). The reaction mixture was stirred at room temperature overnight. Then the mixture was taken-up in EtOAc and washed twice with water and brine. The organic phase was dried over Na2SO4 and the volatiles evaporated at reduced pressure. The crude was purified by flash chromatography eluting with petroleum ether (8) EtOAc (2) using Nynhydrin as stain. Methyl N-{[isopropyl(pent-4-en-1-yl)amino]carbonyl}-3-methyl-L-valinate was obtained as light yellow oil (43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470664B2
Source datasetuspto-grants-2008_12
ORD IDord-fe187bc355c646a99895640ceedc387f
Source noteuspto-grants-2008_12