HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29713Generated: October 29, 2026
Dimethylamine → HCID 59582127, compound
https://huagongshe.com/reaction/29713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-{2-[(3-Bromomethylbenzofuran-2-carbonyl)amino]ethoxy}benzoic acid methyl ester | HCID 66688232 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | HCID 59582127 | HCID 59582127 | — |
Reaction Steps
A solution of 4-{2-[(3-bromomethylbenzofuran-2-carbonyl)amino]ethoxy}-benzoic acid methyl ester (0.340 mol) in chlorobenzene (200 ml) and dichloromethane (800 ml) was added dropwise to a 0-5° C. solution of 2M dimethylamine in tetrahydrofuran (510 ml, 1.022 mol) over 30 minutes with the temperature below 20° C. The resulting mixture was stirred for one hour and allowed to warm to ambient temperature. After completion of reaction, the reaction mixture was washed with 5% potassium carbonate and water. Solvent was distilled at atmospheric pressure until the pot temperature reached 100° C. After cooling to ˜50° C., acetonitrile (400 ml) and ethyl Acetate (400 ml) were added to the pot. The reaction mixture was heated to reflux until all solids dissolved. The reaction mixture was allowed to cool to give 4-{2-[(3-dimethylaminomethyl-benzofuran-2-carbonyl)amino]ethoxy}benzoic acid methyl ester (76.6 g) as an off white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07420089B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-6e7c4934695342f388ab2926659c498e |
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| Source note | uspto-grants-2008_09 |
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