Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 86714715 | HCID 86714715 | — |
| Product | HCID 86714716 | HCID 86714716 | 92% |
Reaction Steps
Allyl bromide (1.30 mL, 15 mmol) was added to a mixture of (E)-but-1-enyldiisobutylamine (1.83 g, 10 mmol) and acetonitrile (5.5 mL) at room temperature under a nitrogen atmosphere, and the mixture was then stirred at an external temperature of 60° C. for 15 hours. The reaction mixture was cooled to room temperature and then concentrated under reduced pressure to obtain the title compound (2.79 g, 92%) as a red purple solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206104B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-4c8fe62e050845f6bc7cdde7866ffce2 |
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| Source note | uspto-grants-2015_12 |
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