HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427617Generated: November 3, 2026
Ethyl Acetate → 2-(4-Chloro-benzyl)-7-iodo-2,3-dihydro-isoindol-1-one
https://huagongshe.com/reaction/2427617
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorobenzylamine | HCID 66036 | — |
| Reactant | Methyl 2-(bromomethyl)-6-iodobenzoate | HCID 11268261 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(4-Chloro-benzyl)-7-iodo-2,3-dihydro-isoindol-1-one | HCID 57949727 | 39.1% |
Reaction Steps
A mixture of 2-bromomethyl-6-iodo-benzoic acid methyl ester (0.200 g, 0.56 mmol), 4-chloro-benzylamine (0.7 mmol), and K2CO3 (0.166 g, 1.2 mmol) in toluene (5 mL) was heated with stirring at 100° C. for 2 h. Workup and silica gel column chromatography using 30% ethyl acetate in hexane afforded 2-(4-chloro-benzyl)-7-iodo-2,3-dihydro-isoindol-1-one (0.084 g, 39%). 1H NMR (300 MHz, CDCl3): δ (ppm) 4.16 (s, 2H), 4.75 (s, 2H), 7.16-7.40 (m, 6H), 7.92 (d, 1H). GC-MS: m/z 367 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968570B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-103cedd473b84096a8bab38fc8112d42 |
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| Source note | uspto-grants-2011_06 |
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