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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454034Generated: October 30, 2026

Phosphorus oxychloride → Ethyl(4-methyl-2-phenyl-1,3-oxazol-5-yl)acetate

https://huagongshe.com/reaction/1454034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 4-benzamido-3-oxopentanoateHCID 21942725—
SolventDimethylformamideHCID 6228—
ProductEthyl(4-methyl-2-phenyl-1,3-oxazol-5-yl)acetateHCID 1411575448.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a crude mixture of ethyl 4-(benzoylamino)-3-oxopentanoate (0.6 g, 2.28 mmol) in DMF (4 mL) at rt was added POCl3(1.04 g, 6.84 mmol). The resulting solution was heated at 90° C. for 1 h, then cooled down to rt, and poured into ice for 30 minutes. The aqueous solution was carefully added to a saturated aqueous solution of NaHCO3. Phases were separated with EtOAc and the combined organic extracts were dried over MgSO4, and the solvent removed under reduced pressure. The crude material was purified on Biotage small column using a solvent gradient of 0 to 50% EtOAc/Hexane. Gave ethyl (4-methyl-2-phenyl-1,3-oxazol-5-yl)acetate (0.269 g 48% yield) as yellowish oil. ES-MS m/z 246.2 ((MH)+); HPLC RT (min) 2.77; 1H NMR (CDCl3) δ 8.01-7.98 (m, 2H), 7.45-7.41 (m, 3H), 4.20 (q, 2H), 3.71 (s, 2H), 2.21 (s, 3H), 1.28 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476742B2
Source datasetuspto-grants-2009_01
ORD IDord-624c8ac674184b59a8498ec0e727ebac
Source noteuspto-grants-2009_01