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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968415Generated: October 28, 2026

Methyl iodide → Methyl 2-(4(S)-phenyloxazolidin-2-on-3-yl)propanoate

https://huagongshe.com/reaction/1968415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 10609791HCID 10609791—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4(S)-phenyloxazolidin-2-on-3-yl)propanoateHCID 66587141—

Reaction Conditions

Temperature-70 °C

Reaction Steps

A solution of Example 2A (1 g, 4.25 mmol) in 10 mL of anhydrous THF at −78° C. was treated with 4.68 mL (4.68 mmol) of a 1 M solution of lithium bis(trimethylsilyl)amide in THF. The reaction mixture was stirred for 1 h. at about −70° C. before adding MeI (1.59 mL, 25.51 mmol). Upon complete conversion of the azetidinone, the reaction was quenched with saturated aqueous NH4Cl and partitioned between EtOAc and water. The organic layer was washed sequentially with saturated aqueous sodium bisulfite, and saturated aqueous NaCl. The resulting organic layer was dried (MgSO4) and evaporated to afford the title compound (a mixture of diasteromers) as a white solid (1.06 g, 93%); 1H NMR (CDCl3) δ 1.07/1.53 (d/d, J=7.5 Hz, 3H), 3.59/3.74 (s/s, 3H), 3.85/4.48 (q/q, J=7.5 Hz, 1H), 4.10-4.14 (m, 1H), 4.60-4.64/4.65-4.69 (m/m, 1H), 4.88-4.92/4.98-5.02 (m/m, 1H), 7.24-7.40 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426400B2
Source datasetuspto-grants-2013_04
ORD IDord-06375c0a8e8c4deba35f231081032837
Source noteuspto-grants-2013_04