HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimellitic anhydride → 2-[4-Allyloxy-3-(5-phenylbenzoxazol-2-yl)phenyl]-1,3-dioxo-2,3-dihydro-1h-isoindole-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimellitic anhydride | HCID 11089 | — |
| Reactant | 2-(5-Amino-2-allyloxyphenyl)-5-phenylbenzoxazole | HCID 21884308 | — |
| Product | 2-[4-Allyloxy-3-(5-phenylbenzoxazol-2-yl)phenyl]-1,3-dioxo-2,3-dihydro-1h-isoindole-5-carboxylic acid | HCID 21884307 | — |
Reaction Steps
Prepared by the method of Example 1b), from 2-(5-amino-2-allyloxyphenyl)-5-phenylbenzoxazole (190 mg, 0.55 mmol) and 1,2,4-benzenetricarboxylic anhydride (106 mg, 0.55 mmol) the title compound was obtained (102 mg, 36%). 1H NMR (DMSO) δ 8.57(m, 1H), 8.35(dd, 1H), 8.37(s, 1H), 8.13(d, 1H), 7.94(m, 3H), 7.77(d, 1H), 7.63(m, 3H), 7.35(m, 4H), 6.04(m, 1H), 5.49(dd, 1H), 5.33(dd, 1H), 4.77(d, 2H). MS 517 m/z (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138425B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-88420af8b1874ef4abbea5ef2b9af9be |
| Source note | uspto-grants-2006_11 |