HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl iodide → 3,5-Di-tert-butyl-2-[(allylamino)methyl]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochloride | HCID 45259771 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,5-Di-tert-butyl-2-[(allylamino)methyl]phenol | HCID 10423542 | — |
Reaction Steps
To 0.705 g (2.99 mmol) of the product of Example 19 in 15 mL of CH2Cl2 was added 1 g of solid NaHCO3 followed by 0.525 g (3.12 mmol) of allyl iodide. The reaction mixture was stirred overnight at room temperature, then filtered and evaporated in vacuo. The residue was purified on a silica gel flash chromatography column eluted with 0-1% MeOH in CH2Cl2. Evaporation of the purified fractions and drying in vacuo afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589127B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-4efc7109ec8541debbe089c7257ecc77 |
| Source note | uspto-grants-2009_09 |