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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802085Generated: November 2, 2026

Acetic Anhydride → HCID 86642929, compound

https://huagongshe.com/reaction/1802085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPropanoic acid, 2-nitro-, ethyl esterHCID 97978—
ReactantHCID 67408090HCID 67408090—
SolventDimethylformamideHCID 6228—
ProductHCID 86642929HCID 8664292970%

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of 6-Heptyloxy-quinoline 1-oxide (500 mg, 0.002 mol) and acetic anhydride (0.255 mL, 0.00270 mol) in N,N-dimethylformamide (5 mL, 0.06 mol) was added to a solution of ethyl 2-nitropropionate (284 mg, 0.00193 mol) in DMF (2 mL) at at 23° C. dropwise. The reaction mixture was then stirred at 23° C. for 12 hours. The reaction mixture was then heated at 50° C. for 6 hours. Solvent was removed under vacuum, and the residue was treated with Na2CO3 (sat), and DCM. Organic layer was collected, and dried over Na2SO4. The mixture was then purified via chromatography (SiO2, 24 g, ethyl acetate/hexanes 0-35%) to give a pure product 523 mg (70%). 1H NMR (CHLOROFORM-d) δ: 8.09 (d, J=8.5 Hz, 1H), 7.95 (d, J=9.0 Hz, 1H), 7.52 (d, J=8.8 Hz, 1H), 7.39 (dd, J=9.3, 2.5 Hz, 1H), 7.08 (d, J=2.5 Hz, 1H), 4.40 (q, J=7.0 Hz, 2H), 4.09 (t, J=6.5 Hz, 2H), 2.40 (s, 3H), 1.82-1.93 (m, 2H), 1.45-1.56 (m, 2H), 1.26-1.44 (m, 9H), 0.92 (t, J=6.7 Hz, 3H). MS (M+1): 389.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349849B2
Source datasetuspto-grants-2013_01
ORD IDord-d18159d8512c4a73a7a697607fb49d5c
Source noteuspto-grants-2013_01