Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl 5-bromo-2-ethylthiophene-3-carboxylate | HCID 68515411 | — |
| Reactant | HCID 178420663 | HCID 178420663 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68511351 | HCID 68511351 | 80% |
Reaction Steps
To a solution of ethyl 5-bromo-2-ethylthiophene-3-carboxylate (5.00 g) synthesized in Example 69 (4) in tetrahydrofuran (50 mL) was added dropwise 1.0M isopropylmagnesium bromide-tetrahydrofuran solution (28.5 mL) at −40° C., and the mixture was stirred for 1.5 hr under an argon atmosphere. Isobutylaldehyde (8.67 mL) was added dropwise, and the mixture was stirred at −40° C. for 1 hr and at room temperature for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. To a solution of the residue in trifluoroacetic acid (50 mL) was added triethylsilane (9.10 mL), and the mixture was stirred at room temperature for 3 hr, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:24, volume ratio) to give the title compound (3.67 g, 80%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08309580B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-522caf57114640d28f36f0a9b59bf312 |
|---|
| Source note | uspto-grants-2012_11 |
|---|