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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520768Generated: October 30, 2026

Citric Acid → HCID 10944665, compound

https://huagongshe.com/reaction/520768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDimethylamineHCID 674—
ReactantWaterHCID 962—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBoc-L-ValineHCID 83693—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDichloromethaneHCID 6344—
ProductHCID 10944665HCID 10944665—

Reaction Steps

EDC.HCl (4.22 g, 22.0 mmol), reagent grade CH2Cl2 (80 mL), HOBt.H2O (3.36 g, 22.0 mmol), and Boc-Val-OH (4.34 g, 20.0 mmol) are added successively at 22° C. under air to a 250 mL round bottom flask equipped with a stir bar. The light yellow solution is allowed to stir for five minutes and dimethylamine (40 wt % in H2O, 5.3 mL, 50 mmol) is added drop-wise over one minute. The flask with the resulting light yellow solution is sealed with a rubber septum and allowed to stir for 12 h at 22° C. An aqueous solution of citric acid (10 wt %, 80 mL) is then added and the mixture is allowed to stir for 0.5 h during which time a white precipitate is formed. The precipitate is removed by filtration and the resulting two layers are separated. The organic layer is washed sequentially with an aqueous solution of citric acid (10 wt %, 80 mL), a saturated aqueous solution of NaHCO3 (80 mL), and brine (80 mL) and is dried over Na2SO4 to give (S)-tert-butyl(1-(dimethylamino)-3-methyl-1-oxobutan-2-yl)carbamate (S2) as pale yellow oil, which is employed without purification in the subsequent deprotection.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328061B2
Source datasetuspto-grants-2016_05
ORD IDord-79c93cd904c44279bb60e6b263115db3
Source noteuspto-grants-2016_05