HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Isopropylaniline → HCID 57429433, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Isopropylaniline | HCID 7464 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18510925 | HCID 18510925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57429433 | HCID 57429433 | 75.1% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
A mixture of ethyl 2-(bromomethyl)-5-nitrobenzoate (1.88 g, 6.52 mmol), 4-isopropylaniline (1.11 mL, 7.83 mmol) and N,N-diisopropylethylamine (1.36 mL, 7.83 mmol) in ethanol (75 mL) was heated in a sealed tube at 110° C. overnight. After this time, the mixture was cooled to room temperature and the solid collected by filtration to afford 2-(4-isopropylphenyl)-6-nitroisoindolin-1-one (1.45 g, 75%) as a yellow solid: mp 225-227° C.; 1H NMR (300 MHz, CDCl3) δ 8.77 (d, J=2.0 Hz, 1H) 8.48 (dd, J=8.3, 2.1 Hz, 1H), 7.76-7.69 (m, 3H), 7.32 (d, J=8.6 Hz, 2H), 2.94 (sept, J=6.9 Hz, 1H), 1.28 (d, J=6.9 Hz, 6H); ESI MS m/z 297 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08110681B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-02ab4ca4a8034b3297fc409504666fe7 |
| Source note | uspto-grants-2012_02 |