HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113732Generated: October 31, 2026
Sulfuric Acid → 2-(Thiophen-2-ylmethyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/2113732
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-[[(2-Thienylmethyl)amino]carbonyl]benzoic acid | HCID 17810161 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Thiophen-2-ylmethyl)isoindoline-1,3-dione | HCID 3354154 | 70% |
Reaction Steps
A solution of 2-aminomethyl-thiophene (2.1 ml, 20.5 mmol) in CHCl3 (25 ml) is treated with phthalic anhydride (3.0 g, 20.5 mmol) at r.t. for 5 min, then at reflux for 20 min, whereupon a white powder precipitated out. This powder is collected by filtration and dried in vacuo to give N-thiophen-2-ylmethyl-phthalamic acid (4.42 g, 83%) as white crystals. An aliquot of this phthalamic acid (2.13 g, 8.12 mmol) is dissolved in MeOH (12 ml), treated with H2SO4 (440 μl, 8.25 mmol) and heated to reflux for 1.5 h, whereupon a white powder precipitated out. This powder is collected by filtration and dried in vacuo to give 1.38 g (70%) of the title phthalimide as white crystals: 1H NMR (DMSO-d6) δ7.92-7.82 (m., 4H), 7.42 (dd, J=5.1, 1.2 Hz, 1H), 7.08 (dd, J=4.0, 0.8 Hz, 1H), 6.95 (dd, J=5.1, 3.5 Hz, 1H), 4.92 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07432286B1 |
|---|
| Source dataset | uspto-grants-2008_10 |
|---|
| ORD ID | ord-9c3c9a1407834b048a3980fa3ea33418 |
|---|
| Source note | uspto-grants-2008_10 |
|---|