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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260460Generated: October 30, 2026

Butyl bromide → HCID 135609944, compound

https://huagongshe.com/reaction/2260460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl bromideHCID 8002—
Reactant1,3,5-TriazineHCID 9262—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 135838255HCID 135838255—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 135609944HCID 135609944—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a 500 mL round bottomed flask equipped with a magnetic stirrer, condenser and nitrogen atmosphere are charged 2.0 g (4.2 mmol) of 2,4-bis-(2,4-dihydroxyphenyl)-6-[4-(phenylthio)phenyl]-s-triazine, 0.58 g (4.2 mmol) of potassium carbonate and 30 mL of N,N-dimethylformamide. The mixture is heated to 90° C., and the s-triazine compound dissolves readily. Bromobutane (4.5 mL, 42.0 mmol) is added all at once. The reaction mixture is heated at 90° C. for 2.5 hours and then stirred at room temperature overnight yielding a yellow precipitate. Chilled water is added and the yellow precipitate is isolated by vacuum filtration to give 2.74 g of crude product. The crude product is purified by flash chromatography with 1:1 heptane:ethyl acetate to afford 0.26 g (10%) yield of the title compound as a yellow solid; mp>250°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05476937
Source datasetuspto-grants-1995_12
ORD IDord-772c83da69214f39be12384f9f82a647
Source noteuspto-grants-1995_12