HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Tolunitrile → HCID 178436103, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Tolunitrile | HCID 7724 | — |
| Reactant | 2-Ethylaniline | HCID 11357 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178436103 | HCID 178436103 | — |
Reaction Steps
Procedure as described for Amidine I using the following amounts: 6.18 mL of 2-ethylaniline (50.0 mmol); 25.0 mL of 2.0 M butyllithium (50.0 mmol), 5.86 g of 4-methylbenzonitrile (50.0 mmol). After refluxing overnight, the solution was dark brown. Addition of water yielded a yellow solution with suspended solid. Solution was filtered and taken to dryness. The residue was treated with 75 mL of pentane, stirred overnight, and filtered yielding 10.51 g (88%) of light yellow solid. 1H NMR (400 MHz, CDCl3): 7.79 (d, 2H), 7.25 (d, 3H), 7.17 (t, 1H), 7.02 (t, 1H), 6.86 (d, 1 H), 4.68 (s, 2H), 2.57 (q, 2H), 2.41 (s, 3H), 1.17 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09283555B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-ba84f3ca8c47404ba4ea89900700b6ca |
| Source note | uspto-grants-2016_03 |