HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Tolunitrile → HCID 178425629, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Tolunitrile | HCID 7724 | — |
| Reactant | 2-tert-Butylaniline | HCID 80574 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178425629 | HCID 178425629 | 84% |
Reaction Steps
Procedure as described for Amidine I using the following amounts: 7.80 mL of 2-t-butylaniline (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 an orange 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 11.14 g (84%) of off-white material. 1H NMR (400 MHz, CDCl3): 7.82 (d, 2H), 7.41 (d, 1H), 7.27 (d, 2H), 7.17 (t, 1H), 7.00 (t, 1H), 6.82 (d, 1 H), 4.75 (s, 2H), 2.42 (s, 3H), 1.40 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09283555B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-d70594401e0f41e38b27f6204d006976 |
| Source note | uspto-grants-2016_03 |