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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635848Generated: October 30, 2026

1-Bromo-4-phenylbutane → HCID 467105, compound

https://huagongshe.com/reaction/635848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-phenylbutaneHCID 259668—
ReactantMagnesiumHCID 5462224—
Reactant174209-00-8HCID 21256490—
SolventDiethyl EtherHCID 3283—
ProductHCID 467105HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191124B1
Source datasetuspto-grants-2001_02
ORD IDord-4c5141791993417d902c22515a706ab2
Source noteuspto-grants-2001_02