Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453114Generated: October 31, 2026

Water → 5-(Bromomethyl)-3-(4-chloro-2-methoxyphenyl)-1,2,4-thiadiazole

https://huagongshe.com/reaction/453114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphorus tribromideHCID 24614—
Reactant(3-(4-Chloro-2-methoxyphenyl)-1,2,4-thiadiazol-5-yl)methanolHCID 59549528—
SolventTolueneHCID 1140—
Product5-(Bromomethyl)-3-(4-chloro-2-methoxyphenyl)-1,2,4-thiadiazoleHCID 5954953164%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of (3-(4-chloro-2-methoxyphenyl)-1,2,4-thiadiazol-5-yl)methanol (0.08 g, 0.31 mmol) in toluene (4 ml) was added PBr3 (49 μl, 0.47 mmol) and the resulting reaction mixture was heated at 60° C. for 2 h. After the completion of the reaction (TLC monitoring), the reaction mixture was cooled to 0° C., added water (50 ml) and extracted with ethyl acetate (3×50 ml). The combined organics was washed with saturated NaHCO3 solution, dried over Na2SO4, filtered and concentrated under vacuum. The crude residue was purified over silica gel (100-200 M, 5% EtOAc-Hexane) to get the desired product (0.063 g, 64%). MS: 319 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492414B2
Source datasetuspto-grants-2013_07
ORD IDord-8ad3327282d046898f49098c9cd5add3
Source noteuspto-grants-2013_07