HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971923Generated: October 30, 2026
Dimethylformamide → HCID 21312568, compound
https://huagongshe.com/reaction/971923
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzimidazol-2-one | HCID 162542 | — |
| Reactant | Methyl 6-Bromohexanoate | HCID 4170292 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21312568 | HCID 21312568 | — |
Reaction Steps
13.4 g (0.1 mol) of benzimidazolone are reacted with 50.2 g (0.24 mol) of methyl 6-bromohexanoate in a solvent mixture of 100 ml of dimethylformamide and 100 ml of benzene, 15.2 g of dry potassium carbonate powder being used as the acid acceptor. The reaction is carried out at 98°-99° C., whilst stirring well, the water formed during the reaction being removed azeotropically. Thereafter, the hot reaction mixture is filtered and the filtrate is concentrated to dryness. A yellowish oil (39.0 g), which completely crystallises on standing, is obtained in quantitative yield. The purification can be carried out in the customary manner. The product thus prepared shows a proton magnetic resonance spectrum which agrees with the following structure: ##STR20##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04161603 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-fa3441603889467e9d3d2584a65c2e0e |
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| Source note | uspto-grants-1979_07 |
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