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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288653Generated: November 1, 2026

2,6-Lutidine → HCID 53655786, compound

https://huagongshe.com/reaction/1288653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantButyl iodideHCID 10962—
ReactantHCID 53862388HCID 53862388—
ProductHCID 53655786HCID 53655786—

Reaction Conditions

Temperature135 °C

Reaction Steps

N-(4-Carboxyethylphenyl)alanine ethyl ester (2.6 g, 0.01 mol), n-butyl iodide (1.8 g, 0.01 mol) and 2,6-lutidine (1.5 g, 0.04 g) were sealed in a glass tube. The contents of the tube were heated at 135° C. for 48 h. The tube was then cooled and the contents were partitioned between 200 mL ethyl acetate and 200 mL brine. The organic layer was separated, dried over anhyd. sodium sulfate and concentrated at reduced pressure. The resulting oil was charged onto a silica gel column, and eluted with heptane:THF (4:1). The desired ester was isolated as a light yellow oil (0.5 g, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747236
Source datasetuspto-grants-1998_05
ORD IDord-3c2503722b0f44279fd739b3e04b7b9c
Source noteuspto-grants-1998_05