HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl iodide → HCID 54253050, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 53903419 | HCID 53903419 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54253050 | HCID 54253050 | — |
Reaction Steps
N-(4-Methylthiophenyl)alanine ethyl ester (10.0 g, 42.0 mmol), n-butyl iodide (7.9 g, 42 mmol) and potassium carbonate were added to 150 mL of acetonitrile and the mixture was heated at reflux for 48 h under a nitrogen atmosphere. The reaction mixture was cooled and then partitioned between 300 mL ethyl acetate and 200 mL brine. The organic layer was separated, washed with 100 mL brine, 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 (5:1). The desired ester was isolated as a yellow oil (3.0 g, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05747235 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-ef903a1a30a14706bbb8e2bcdf2b2001 |
| Source note | uspto-grants-1998_05 |