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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733305Generated: October 26, 2026

Allyl iodide → 3,5-Di-tert-butyl-2-[(allylamino)methyl]phenol

https://huagongshe.com/reaction/733305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Aminomethyl)-3,5-di-tert-butylphenol hydrochlorideHCID 45259771—
SolventDichloromethaneHCID 6344—
Product3,5-Di-tert-butyl-2-[(allylamino)methyl]phenolHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589127B2
Source datasetuspto-grants-2009_09
ORD IDord-4efc7109ec8541debbe089c7257ecc77
Source noteuspto-grants-2009_09