HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-4-phenylbutane → HCID 467105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-4-phenylbutane | HCID 259668 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 174209-00-8 | HCID 21256490 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 467105 | HCID 467105 | — |
Reaction Steps
Magnesium (0.15 g) in ether (15 mL) was treated with 1-bromo-4-phenylbutane (prepared by the procedure described in Kamijo et al., Chem. Phar. Bull., 1983, 31, 4189) (1.50 g) at 0° and the mixture was reacted at 25° for 2.5 hours. The suspension was cooled to 0°, solid 3-Methylimidazo[2,1-b]thiazole-5-carboxaldehyde (FIG. C-6) (0.332 g) was added and the mixture was reacted at 25° for 3 hours. The solution was decanted into 5% NH4Cl solution and extracted with ethyl acetate. The extract was dried, evaporated and the residue (0.55 g) was crystallized from acetonitrile solution to yield pure 3-Methyl-α-(4-phenylbutyl)imidazo-[2,1-b]thiazole-5-methanol (FIG. C-7) (0.39 g), m.p. 120-121°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191124B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-4c5141791993417d902c22515a706ab2 |
| Source note | uspto-grants-2001_02 |