Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531874Generated: October 31, 2026

3-Amino-3-(4-methoxyphenyl)propanoic acid → HCID 21250922, compound

https://huagongshe.com/reaction/1531874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Amino-3-(4-methoxyphenyl)propanoic acidHCID 585889—
ReactantHCID 86750389HCID 86750389—
SolventAcetic AcidHCID 176—
ProductHCID 21250922HCID 2125092292%

Reaction Steps

A stirred mixture of 2,3,4,5-tetrachlorophthalic acid anhydride (2.85 g, 10.0 mmol) and 3-amino-3-(4-methoxyphenyl)propionic acid (1.95 g, 10.0 mmol) in 25 mL of acetic acid under nitrogen was heated to reflux for 4.5 hours. A solid formed as the reaction mixture cooled. The resulting slurry was filtered and the solid dried in vacuo (60° C., <2 mm) to afford 4.24 g (92%) of 3-(2,3,4,5-tetrachlorophthalimido)-3-(4-methoxyphenyl)-propionic acid as an off-white solid contaminated with ˜1% acetic acid: mp 235.6-238° C.; 1H NMR (DMSO-d6) δ12.44 (br s, 1H, COOH), 7.36 (d, J=8.7 Hz, 2H), 6.90 (d, 1 H, J=8.7 Hz), 5.64 (m, 1H), 3.72 (s, 3H), 3.35 (m, 2H); 13C NMR (DMSO-d6) δ171.5, 163.0, 158.8, 138.4, 129.9, 128.6, 128.2, 127.6, 113.8, 55.0, 50.2, 35.6. Anal. Calcd for C18H11NO5Cl4. Theory: C, 46.68; H, 2.39; N, 3.02. Found: C, 46.58; H, 2.31; N,2.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200987B1
Source datasetuspto-grants-2001_03
ORD IDord-cb0831441c4f4b8da8b0ea4e1b6cc013
Source noteuspto-grants-2001_03