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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588116Generated: October 30, 2026

Tert-butyl (s)-(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate → (S)-tert-butyl(2-oxo-1-phenylpropyl)carbamate

https://huagongshe.com/reaction/588116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (s)-(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamateHCID 10968398—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product(S)-tert-butyl(2-oxo-1-phenylpropyl)carbamateHCID 90251117—

Reaction Steps

At 0° C., to a solution of (S)-tert-butyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate (0.9 g, 3.06 mmol) in anhydrous THF (15 mL), was added MeMgBr (3M solution in Et2O, 2.0 mL, 6.1 mmol) and resultant mixture was allowed to warm and stirred at ambient temperature. After 2 hrs, the reaction was carefully quenched with saturated aqueous NH4Cl solution (10 mL), and the organic contents were extracted with CH2Cl2 (3×25 mL). The volatiles were removed under reduced pressure to afford (S)-tert-butyl(2-oxo-1-phenylpropyl)carbamate. The compound obtained is pure and no further purification is necessary. 1H NMR (300 MHz, CDCl3) δ 7.40-7.33 (m, 5H), 5.88 (bs, 1H), 5.28 (bs, 1H), 2.08 (s, 3H), 1.41 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226922B2
Source datasetuspto-grants-2016_01
ORD IDord-259ca1249f5f4c768d4f8d468bd07177
Source noteuspto-grants-2016_01