HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751054Generated: October 27, 2026
Dimethylformamide → N-(7-Cyano-2-methyl-benzofuran-4-yl)-2,2-dimethylpropionamide
https://huagongshe.com/reaction/751054
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | N-(2-Allyl-4-cyano-3-hydroxyphenyl)-2,2-dimethylpropionamide | HCID 59754237 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(7-Cyano-2-methyl-benzofuran-4-yl)-2,2-dimethylpropionamide | HCID 59754271 | 60.3% |
Reaction Steps
To a solution of compound 10D (0.5 g, 1.94 mmol) in a mixed solvent of DMF (2.5 mL) and water (1.9 mL) was added Cu(OAc)2 (1.057 g, 5.82 mmol), followed by a 10 M aqueous solution of LiCl (0.58 mL, 5.8 mmol) and PdCl2 (34.3 mg, 0.194 mmol). The resulting suspension was heated to 100° C. for 1 h. After cooling to rt, the reaction mixture was poured into ice/water, and extracted with EtOAc (3×). The combined EtOAc extracts were washed with brine, dried (Na2SO4), and concentrated under reduced pressure. The crude product was chromatographed (silica gel) eluting with 10% to 50% EtOAc/hexane to furnish the title compound (0.3 g) as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405234B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-d5eb9ed7fcf847c6b4c279129ac6499f |
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| Source note | uspto-grants-2008_07 |
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