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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028602Generated: November 4, 2026

Hydrochloric Acid → (1,1-Dimethyl-2-oxoethyl)carbamic acid benzyl ester

https://huagongshe.com/reaction/1028602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantBenzyl {2-[methoxy(methyl)amino]-1,1-dimethyl-2-oxoethyl}carbamateHCID 22031370—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(1,1-Dimethyl-2-oxoethyl)carbamic acid benzyl esterHCID 14578675—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Diisobutylaluminum hydride (1.77 mL, 1M solution in toluene, 0.708 mmol) was added to a stirred solution of benzyl {2-[methoxy(methyl)amino]-1,1-dimethyl-2-oxoethyl}carbamate (198.5 mg, 0.708 mmol) in dry THF (7.1 mL) at −78° C. under N2. The reaction was stirred at −78° C. for 4 h. MeOH (100 mL) and 1N HCl (250 μL) were added and the reaction was allowed to warm to room temperature. The mixture was diluted with Et2O (50 mL) and washed with 1N HCl (2×50 mL), 50% saturated NaHCO3 (50 mL) and water (50 mL), then dried (MgSO4) and concentrated in vacuo to give benzyl (1,1-dimethyl-2-oxoethyl)carbamate. Rf=0.40 (20% EtOAc in hexanes). LCMS calc.=244.1; found=244.1 (M+Na)+. 1H NMR (500 MHz, CDCl3) δ 9.43 (s, 1H), 7.38-7.30 (m, 5H), 5.34 (s, 1H), 5.09 (s, 2H), 1.37 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735435B2
Source datasetuspto-grants-2014_05
ORD IDord-89c55300f6e247e09fb1213e8aabe7f5
Source noteuspto-grants-2014_05