HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110121Generated: October 30, 2026
Water → 4-[(3-Butyl-4-cinnolinyl)-methyl]-benzonitrile
https://huagongshe.com/reaction/1110121
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 19595374 | HCID 19595374 | — |
| Catalyst | HCID 69459885 | HCID 69459885 | — |
| Catalyst | Nickel diphenyl phosphino propane chloride | HCID 86747958 | — |
| Product | 4-[(3-Butyl-4-cinnolinyl)-methyl]-benzonitrile | HCID 18999075 | — |
Reaction Steps
100 mg of nickel diphenyl phosphino propane chloride were added to a solution of 0.87 g of 3-butyl-4-chloro cinnoline of Step C and 30 ml of tetrahydrofuran and the mixture was refluxed. 10 ml of a 0.5 M solution in tetrahydrofuran of 4-bromomethyl benzonitrile zinc (prepared as Knochel, J. Org. Chem., (1988), Vol. 53. p. 5789 to 5791) were added, followed by stirring for one hour at 50° C., then pouring into ice-cooled water. The solution was alkalized by the addition of ammonium hydroxide, concentrated and extracted with ethyl acetate. The extracts were washed with water, dried and evaporated to dryness. The residue was chromatographed on silica (eluant: ethyl acetate - hexane (1-1)) to obtain 680 mg of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05324839 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-73f3954ac35c44d2b1f2aa02d606a599 |
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| Source note | uspto-grants-1994_06 |
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