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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284529Generated: October 29, 2026

Nitrogen → Benzyl (isobutylcarbamoyl)glycinate

https://huagongshe.com/reaction/2284529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTolueneHCID 1140—
ReactantIsovaleric AcidHCID 10430—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantBenzyl 2-aminoacetate hydrochlorideHCID 11701227—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductBenzyl (isobutylcarbamoyl)glycinateHCID 11802184681.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

Charge 3-methylbutanoic acid (106.36 g), toluene (800 ml) and triethylamine (126.46 g) into a 3-neck flask (R1). Heat R1 to 90° C. Add a solution of DPPA (289.3 g) in toluene (400 ml) slowly (Care: N2 released). Stir R1 at 90° C. for 30-60 mins, then cool to 20-30° C. In a separate flask (R2) charge benzyl 2-aminoacetate hydrochloride (200 g), triethylamine (150.54 g), and toluene (1000 ml) and stir at 20-30° C. for 1-2 hours. Add the R1 mixture into R2 drop wise slowly via addition funnel at 20-30° C. and stir for 1-2 hours. Slowly add the reaction mixture to water (2000 ml) with vigorous stirring. Separate the organic and extract the aqueous layer with EtOAc (2×1000 ml). Combine the organic layers and wash with 1 N hydrochloric acid (1000 ml), then 7% NaHCO3 aq (1000 ml), then water (1000 ml), then 15% brine (1000 ml). Concentrate under reduced pressure. Slurry the residue with heptane (1000 ml) then filter the solid. Dry the filter cake under reduced pressure below 40° C. to give benzyl 2-(isobutylcarbamoylamino)acetate (218 g; 98.1% assay; 81.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145435B2
Source datasetuspto-grants-2015_09
ORD IDord-4a96d76d93b542368f6a8c1074fcd1c6
Source noteuspto-grants-2015_09