HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719802Generated: October 29, 2026
Dimethylformamide → HCID 21887257, compound
https://huagongshe.com/reaction/719802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 605205 | HCID 605205 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21887257 | HCID 21887257 | 96.5% |
Reaction Steps
Oxalyl chloride (7.0 ml, 81 mmol) was added by portions to a solution of 4-(1,3-dimethyl-2-oxo-2,3-dihydro-1H-benzimidazol-5-yl)butanoic acid (20 g, 81 mmol) obtained in Reference Example 136 and dimethylformamide (1 ml) in tetrahydrofuran under ice-cooling. After stirring at room temperature for 30 minutes, the reaction mixture was concentrated, the reaction residue was dissolved in nitroethane, and aluminum chloride (21.6 g, 162 mmol) was added by portions under ice-cooling. After stirring at room temperature for 30 minutes, the reaction mixture was poured into ice (500 g), extracted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure, and the residue was crystallized from ethanol-diethyl ether to give the title compound as colorless crystals (18.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132547B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-fa926753253a4e7babff2d74a1b3582b |
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| Source note | uspto-grants-2006_11 |
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