HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propyltriphenylphosphonium bromide → 4-(5-But-1-enyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propyltriphenylphosphonium bromide | HCID 80374 | — |
| Reactant | 3-(3,3-dimethyl-1-oxo-isochroman-4-yl)-3H-imidazole-4-carbaldehyde | HCID 24802690 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-But-1-enyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one | HCID 66906441 | — |
Reaction Steps
To a solution of propyltriphenylphosphonium bromide (0.157 g, 0.41 mmol) in THF (1 mL) at −78° C. is added sodium hexamethyldisilylamide (1M in THF, 0.44 mL, 0.44 mmol) and the mixture is allowed to warm to ambient temperature over 10 min. This solution is cooled to −20° C. and 3-(3,3-dimethyl-1-oxo-isochroman-4-yl)-3H-imidazole-4-carbaldehyde (0.10 g, 0.37 mmol) in THF (0.2 mL) is added. The cooling bath is removed and the mixture is stirred at ambient temperature overnight, then filtered. The filtrate is concentrated in vacuo to give the crude 4-(5-but-1-enyl-imidazol-1-yl)-3,3-dimethyl-isochroman-1-one which is used in the next step without further purification; MS (ESI) m/z 297.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153674B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-72087c82a35f4611ae672d52c11119f3 |
| Source note | uspto-grants-2012_04 |