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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040264Generated: October 27, 2026

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

https://huagongshe.com/reaction/1040264

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 hour, 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 solvent removed under reduced pressure. The crude material was purified on Biotage small column using a solvent gradient of 0 to 50% EtOAc/Hexane. This 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 numberUS08552203B2
Source datasetuspto-grants-2013_10
ORD IDord-80d6daa5e77c4bcca08a834ab42959e8
Source noteuspto-grants-2013_10