HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742326Generated: October 31, 2026
Diisopropylamine → 2-[(4-Methylphenyl)phenylmethylene]propanedinitrile
https://huagongshe.com/reaction/742326
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | 4-Methylbenzophenone | HCID 8652 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[(4-Methylphenyl)phenylmethylene]propanedinitrile | HCID 11265056 | 104.3% |
Reaction Steps
To a solution of 0.85 mL (6 mmol) of diisopropylamine in 11.3 mL of dry tetrahydrofuran, cooled to -78° C., was added 3.5 mL (5.6 mmol) of BuLi and the resulting mixture was stirred for 10 min. Next, 0.34 g (5.1 mmol) of malononitrile dissolved in 1.7 mL of tetrahydrofuran was carefully added and the resulting mixture was stirred for 30 min more. Finally, 1 g (5.1 mmol) of 4-methylbenzophenone in 1.7 mL of tetrahydrofuran was added. The mixture was allowed to warm up to room temperature and then it was heated at reflux for 2 days. Ethyl acetate was added and the resulting solution was washed with water. The aqueous phase was extracted with ethyl acetate and the combined organic phases were dried and the solvent was removed to yield 1.3 g of the desired product as a reddish oil (yield: quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05554624 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-6b7e62966b354958bc2127abb0beea47 |
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| Source note | uspto-grants-1996_09 |
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