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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266069Generated: October 27, 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/2266069

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-isopropyl4,5-dimethoxy-benzylidene)-(1-isopropyl-2-methyl-propyl)-amine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858632B2
Source datasetuspto-grants-2010_12
ORD IDord-f418c2e0a9e94faea33b4ddd580924d5
Source noteuspto-grants-2010_12