Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Methylbenzonitrile | HCID 10721 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67215554 | HCID 67215554 | — |
Reaction Steps
A solution of MeMgBr in ether (12.9 mL, 3.0 M, 38.7 mmol) was added to a solution of diisopropylamine (3.91 g, 38.7 mmol) in toluene (60 mL) at 50° C. The mixture was stirred for 1 h and a white precipitate formed. Next, the mixture was cooled to 0° C. and tolunitrile (4.53 g, 38.7 mmol) was added. The mixture was allowed to warm to room temperature and stirred for 16 h subsequently. The mixture was quenched with water (100 mL). The organic phase was separated from the aqueous phase and the latter was extracted with diethylether (150 mL) twice. The combined organic phases were dried over Na2SO4, filtered and the solvents were removed under reduced pressure giving a sticky residue. This residue was triturated with ligroin giving 4.40 g (52%) pure product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07956140B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-0201ef0769c14625bb6b7d9e0536f371 |
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| Source note | uspto-grants-2011_06 |
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