HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860624Generated: November 2, 2026
Methanol → 5-Bromobenzofuran-2-carboxylic Acid Dibenzylamide
https://huagongshe.com/reaction/1860624
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | 5-Bromobenzo[b]furan-2-carbonyl chloride | HCID 2795534 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Bromobenzofuran-2-carboxylic Acid Dibenzylamide | HCID 9866799 | 77% |
Reaction Steps
A solution of 50 ml of toluene and 7.9 g of dibenzylamine are added dropwise with stirring at 50-60° C. in the course of 10 min. to 5.2 g of 5-bromobenzofuran-2-carbonyl chloride in 100 ml of toluene. A colourless solid is obtained. After dropwise addition is complete, the mixture is additionally stirred at 100-110° C. for a further 3 hours. After cooling to 10° C., the solid product (dibenzylammonium chloride) is filtered off with suction. The filtrate is then treated with a mixture of 150 ml of water and 10 g of sodium carbonate and thoroughly shaken. The organic phase is separated off, washed again with 100 ml of water, dried using sodium sulfate and filtered. The, filtrate is concentrated on a Rotavapor in vacuo to a residue (residue: 9.5 g). After recrystallization from 100 ml of methanol, 6.5 g of product (yield 77%) remain after isolation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06531503B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-04f5167b96d845589dad789600f3e056 |
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| Source note | uspto-grants-2003_03 |
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