2-Bromoethanol → HCID 21717685, compound

To a solution of 5-(3,4-Dichloro-phenyl)-3-(3-[1,3]dioxolan-2-yl-phenyl)-1H-[1,2,4]triazole mixture of tautomers) (400 mg, 0.31 mmol) in acetonitrile (5 ml) was added 2-bromoethanol (156 μl, 2.21 mmol) and BEMP on poystyrene resin support (2.3 mmol/g, 960 mg). This mixture was shaken at r.t. until the starting material had been consumed (5 d), then aminomethyl polystyrene (1.1 mmol/g, 147 mg) was added and the mixture shaken for a further 2 h at r.t. The mixture was then filtered, washed with acetonitrile and evaporated to afford an isomeric mixture of alkylated acetals which were chromatographically separated over SiO2 (Merck 230-400 Mesh) eluting with EiOAc/nHexane (1:4). The purified isomer was dissolved in THF (3 ml) and treated with 4N HCl (0.3 ml) at r.t. for 3 h, then the mixture was adjusted to pH 9 with NaHCO3, and the aqueous phase extracted twice with EtOAc. The organic phases were combined, dried, filtered and evaporated to afford the title aldehyde as a light yellow solid (45 mg, 11% yield), MS: m/e=362.2 (M+H+). The position of alkylation on the triazole ring was assigned by 1H-NMR, nOe spectroscopy.

1. customhad been consumed (5 d)
2. additionaminomethyl polystyrene (1.1 mmol/g, 147 mg) was added
3. stirringthe mixture shaken for a further 2 h at r.t
4. filtrationThe mixture was then filtered
5. washwashed with acetonitrile
6. customevaporated
7. customto afford
8. customwere chromatographically separated over SiO2 (Merck 230-400 Mesh)
9. washeluting with EiOAc/nHexane (1:4)
10. dissolutionThe purified isomer was dissolved in THF (3 ml)
11. additiontreated with 4N HCl (0.3 ml) at r.t. for 3 h
12. extractionthe aqueous phase extracted twice with EtOAc
13. customdried
14. filtrationfiltered
15. customevaporated

ORD record

ord-5bdd53cb5a9041abb29e47309148500b

Source dataset

uspto-grants-2001_07

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06265426B1