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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231793Generated: November 1, 2026

Isobutyl chloroformate → Boc-Ile-Pro-OBzl

https://huagongshe.com/reaction/2231793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butoxycarbonyl-L-isoleucineHCID 2724762—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
SolventDimethylformamideHCID 6228—
Solvent4-MethylmorpholineHCID 7972—
ProductBoc-Ile-Pro-OBzlHCID 1430623592%

Reaction Conditions

Temperature-15 °C

Reaction Steps

Boc-Ile-OH (12.01 g, 0.05 mole) in DMF (50 ml) was cooled to 0° C. and NMM (5.49 ml) was added. After cooling the solution to -15° C. isobutylchloroformate (6.48 ml) was added slowly while maintaining the temperature at -15° C. and stirred for 10 minutes at which time HOBt (7.65 g) was added and stirring was continued for additional 10 minutes. A pre-cooled solution of HCl-H-Pro-OBzl (12.09 g, 0.05 mole) in DMF (50 ml) and NMM (5.49 ml) was added to the above solution and the completeness of the reaction was followed by TLC. The reaction mixture was poured into a cold saturated NaHCO3 solution and stirred for one hour. The peptide was extracted into CHCl3 and washed with acid and base (0.5 N NaOH to remove HOBt), and on evaporating the solvent the product was obtained as an oil in 92% yield. Rf1, 0.65. Anal. Calcd. for C23H34N2O5 : C 66.00, H 9.19, N 6.69%. Found: C 65.58, H 8.28, N 7.13%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04783523
Source datasetuspto-grants-1988_11
ORD IDord-1397fcaccb1546d1b928450fe3f865c1
Source noteuspto-grants-1988_11