HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488066Generated: October 31, 2026
HCID 13600230, compound → HCID 90033029, compound
https://huagongshe.com/reaction/1488066
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 13600230 | HCID 13600230 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90033029 | HCID 90033029 | — |
Reaction Steps
Into a 1000-mL three-neck round-bottom flask, which was purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 4-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-imidazole (compound 192.1, 9 g, 42.38 mmol) in tetrahydrofuran (200 mL). This was followed by the addition of n-BuLi (34 mL, 2.5 M in THF) dropwise at −78° C. and stirred for 1 h. To this was added a solution of oxetan-3-one (6.11 g, 84.79 mmol) in tetrahydrofuran (30 mL) dropwise at −78° C. The reaction mixture was stirred for 1 h at −78° C., then quenched with 50 mL of NH4Cl (sat.). The aqueous phase was extracted with 1×600 mL of ethyl acetate. The organic layer was washed with 3×300 mL of brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. This resulted in 13 g (crude) of the title compound as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09428502B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-6182f8135632473e9fe86104c0604d15 |
|---|
| Source note | uspto-grants-2016_08 |
|---|