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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269162Generated: October 31, 2026

Acetic Acid → HCID 69183728, compound

https://huagongshe.com/reaction/1269162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 69184524HCID 69184524—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69183728HCID 6918372881%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (4S)-3-[(4-fluorophenyl)acetyl]-4-isopropyl-1,3-oxazolidin-2-one (2.81 g, 10.6 mmol) in dry THF (40 mL) at −78° C. under argon, was added dropwise 1.0M solution of NaHMDS in THF (11.7 mL, 11.7 mmol) over a period of 10 min. After stirring at −78° C. for 1 h, Mel (3.30 mL, 53.0 mmol) was added. The resulting reaction mixture was stirred at −78° C. for 1 h and −40° C. for 2 h, quenched with HOAc (32 mmol) in ether (20 mL), filtered over celite. The filtrate was concentrated in vacuo and the residue was dissolved in CH2Cl2 (100 mL) and washed with H2O following by brine, dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography (5%–10% EtOAc in hexane) to give 2.40 g (8.60 mmol, 81%) of (4S)-3-[(2S)-2-(4-fluorophenyl)propanoyl]-4-isopropyl-1,3-oxazolidin-2-one: 1H NMR (400 MHz, CDCl3) δ 7.34–7.31 (m, 2H), 7.02–6.96 (m, 2H), 5.13 (q, 1H, J=7.7 Hz), 4.38–4.33 (m, 1H), 4.18–4.13 (m, 2H), 2.48–2.37 (m, 1H), 1.49 (d, 3H, J=7.3 Hz), 0.91 (apparent t, 6H, J=6.9 Hz); ESMS m/e: 280.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199135B2
Source datasetuspto-grants-2007_04
ORD IDord-40287dfc60a84e74af99715bf1cac23d
Source noteuspto-grants-2007_04