HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → (R)-N-Allyl-1-aminoindane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (R)-(-)-1-Aminoindan | HCID 2733933 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-N-Allyl-1-aminoindane | HCID 5326779 | — |
Reaction Steps
To a solution of (1R)-indan-1-amine (1.00 g, 7.51 mmol) and triethylamine (1.52 g, 15.0 mmol) in DCM (75 mL) was added allyl bromide (1.36 g, 11.3 mmol) and the mixture was allowed to stir at ambient temperature for 3 days. An additional 1.5 equivalents of allyl bromide and 0.5 equivalents of triethylamine were then added, and the reaction mixture was stirred an additional 24 hours. LCMS analysis now indicates the reaction mixture is a 27:35:38 mixture of starting material:desired product:bis-allylation product. Use this solution as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552023B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-53dbdc49b1614eab9da7af2681f00f5a |
| Source note | uspto-grants-2013_10 |