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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607039Generated: October 29, 2026

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

https://huagongshe.com/reaction/607039

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 μL) 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 numberUS07915271B2
Source datasetuspto-grants-2011_03
ORD IDord-ae022a2113aa41879680bb92e2821548
Source noteuspto-grants-2011_03