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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173628Generated: October 26, 2026

Ammonium Chloride → Carbamic acid, [(1S)-1-methyl-2-oxopropyl]-, 1,1-dimethylethyl ester (9CI)

https://huagongshe.com/reaction/1173628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamateHCID 11806530—
ReactantAcetone cardiceHCID 18522661—
ReactantHCID 178467906HCID 178467906—
SolventTetrahydrofuranHCID 8028—
ProductCarbamic acid, [(1S)-1-methyl-2-oxopropyl]-, 1,1-dimethylethyl ester (9CI)HCID 14352057—

Reaction Steps

A solution of tert-butyl{(1S)-1-[methoxy(methyl)carbamoyl]ethyl}carbamate (5.26 g) in tetrahydrofuran (300 mL) was cooled with dry ice/acetone under a nitrogen atmosphere, and 1.6 mol/L-methyllithium/diethyl ether solution (38.8 mL) was added. After stirring at the same temperature for 1.5 hr, saturated aqueous ammonium chloride solution (100 mL) was added to the reaction solution, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentration under reduced pressure to give the title compound as a colorless oil (yield: 4.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834051B2
Source datasetuspto-grants-2010_11
ORD IDord-6bde34d1910d43d6aeafcb0970bac879
Source noteuspto-grants-2010_11