Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677244Generated: October 25, 2026

(1-Isopropyl-2-methyl-propyl)-(2,4,5-trimethoxy-benzylidene)-amine → (2-Isopropyl4,5-dimethoxy-benzylidene)-(1-isopropyl-2-methyl-propyl)-amine

https://huagongshe.com/reaction/1677244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Isopropyl-2-methyl-propyl)-(2,4,5-trimethoxy-benzylidene)-amineHCID 59598598—
ReactantHCID 178506895HCID 178506895—
SolventTetrahydrofuranHCID 8028—
Product(2-Isopropyl4,5-dimethoxy-benzylidene)-(1-isopropyl-2-methyl-propyl)-amineHCID 59598696—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (1-isopropyl-2-methyl-propyl)-(2,4,5-trimethoxy-benzylidene)-amine (1.024 g, 3.5 mmol) in 35 ml THF at −78° C. was added isopropyllithium (6.0 mL, 0.7 M in pentane) drop-wise over 5 minutes. The solution was allowed to stir 30 min at −78° C. After warming to room temperature over 45 minutes the mixture was quenched by the addition of 5 mL of 10% NH4Cl and concentrated in vacuo. 100 mL of H2O was added and the mixture was extracted with ethyl acetate, washed with H2O and then brine. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo to give (2-isopropyl-4,5-dimethoxy-benzylidene)-(1-isopropyl-2-methyl-propyl)-amine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008313B2
Source datasetuspto-grants-2011_08
ORD IDord-52e9555fad3d49119d8d1acf5a088caa
Source noteuspto-grants-2011_08