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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421313Generated: October 29, 2026

3-Nitrophthalic anhydride → HCID 9864149, compound

https://huagongshe.com/reaction/1421313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophthalic anhydrideHCID 21631—
Reactant3-Amino-3-(4-methoxyphenyl)propanoic acidHCID 585889—
SolventAcetic AcidHCID 176—
ProductHCID 9864149HCID 986414979%

Reaction Steps

A mixture of 3-nitrophthalic anhydride (1.54, 8.0 mmol) and 3-amino-3-(4-methoxyphenyl)propionic acid (1.56 g, 8.0 mmol) in 15 mL of acetic acid was refluxed for 3.5 h under nitrogen. The reaction was cooled and removed some of the solvent. The slurry was filtered and the solid was dried to afford 2.34 g (79%) of 3-(4-methoxyphenyl)-3-(3-nitrophthalimido)propionic acid as a white powder: mp 178-180° C.; 1H NMR (DMSO-d6, 250 MHz)δ 8.07-8.02 (m, 3H), 7.38 (d, 2H, J=8.7), 6.90 (d, 2H, J=8.7, 5.68-5.07 (m, 1H), 3.72 (s, 3H), 3.48-3.22 (m, 2H); 13C NMR (DMSO-d6)δ 171.6, 165.7, 163.0, 158.8, 144.4, 136.4, 133.0, 130.2, 128.6, 128.5, 127.0, 122.4, 113.9, 55.1, 50.0, 35.8. Anal. Calcd for C18H14N2O7. Theoretical: C, 58.38; H, 3.81; N, 7.56. Found: C, 58.18; H, 3.79; N, 7.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06075041
Source datasetuspto-grants-2000_06
ORD IDord-ac6beef413cb4830986b3859084e9004
Source noteuspto-grants-2000_06