HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640022Generated: November 2, 2026
4-Isopropylaniline → HCID 57429432, compound
https://huagongshe.com/reaction/1640022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Isopropylaniline | HCID 7464 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 2-(bromomethyl)-5-chlorobenzoate | HCID 13272463 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57429432 | HCID 57429432 | 53.1% |
Reaction Steps
A mixture of ethyl 2-(bromomethyl)-5-chlorobenzoate (0.553 g, 1.99 mmol), 4-isopropylaniline (0.269 g, 1.99 mmol) and sodium ethoxide (0.406 g, 5.97 mmol) in ethanol (40 mL) was heated at reflux overnight. After this time, the mixture was cooled to room temperature and concentrated under vacuum. The mixture was partitioned between 1 N HCl and ethyl acetate. The organic layer was separated, washed with 1 N HCl, then with 1:1 water/brine solution, dried over sodium sulfate and filtered. Concentration under vacuum and recrystallization from ethyl acetate afforded 6-chloro-2-(4-isopropylphenyl)isoindolin-1-one (0.302 g, 53%) as an off-white solid: m.p. 206-209° C.; 1H NMR (500 MHz, CDCl3) δ 7.89 (d, J=1.9 Hz, 1H), 7.73 (dt, J=8.6, 2.7 Hz, 2H), 7.55 (dd, J=8.1, 1.9 Hz, 1H), 7.45 (d, J=8.0 Hz, 1H), 7.30 (dt, J=8.5, 2.5 Hz, 2H), 4.83 (s, 2H), 2.96-2.90 (m, 1H), 1.26 (d, 6H); ESI MS m/z 286 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110681B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-18922b1730304cbba908a1f6ff1e29cc |
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| Source note | uspto-grants-2012_02 |
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