Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | HCID 53862388 | HCID 53862388 | — |
| Product | HCID 53655786 | HCID 53655786 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747236 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-3c2503722b0f44279fd739b3e04b7b9c |
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| Source note | uspto-grants-1998_05 |
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