HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618940Generated: October 31, 2026
HCID 4447362, compound → 3-(1H-Benzimidazol-2-yl)-4-chloroaniline
https://huagongshe.com/reaction/1618940
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 4447362 | HCID 4447362 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(1H-Benzimidazol-2-yl)-4-chloroaniline | HCID 278831 | 49.7% |
Reaction Steps
Iron powder (15.42 g, 280 mmol) was added to a solution of amide 1 (15.00 g, 46.7 mmol) in toluene (125 ml) and acetic acid (60 nil). The mixture was heated at 125° C. for about 1 h (completion of the reaction was monitored by LCMS) and the resulting crude mixture was filtered through a cotton wool plug (to remove iron particles). The crude solution was evaporated to dryness, diluted with EtOAc, washed with saturated NaHCO3 then brine, dried over MgSO4, filtered, and concentrated at reduced pressure. The resulting brown solid was redissolved in CH2Cl2 and few drops of hexane were added to form a solid which was isolated by filtration to give 2 (5.66 g, 42%) as a beige solid: 1H NMR (CD3OD) δ 7.64 (broad s, 2H), 7.30-7.26 (m, 3H), 7.13 (app d, 1H), 6.84 (dd, 1H); MS (ES, positive mode): 244 [M++1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772275B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-6376232c5f844bbd86858bf177d15412 |
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| Source note | uspto-grants-2014_07 |
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