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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417757Generated: November 1, 2026

Allyl bromide → HCID 56626424, compound

https://huagongshe.com/reaction/2417757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 178448763HCID 178448763—
SolventChloroformHCID 6212—
SolventSodium HydroxideHCID 14798—
ProductHCID 56626424HCID 5662642440%

Reaction Steps

26.6 g (0.22 mol) of allyl bromide were added to a solution of 43.6 g (0.2 mol) of 4-amino-6-fluoro-tert.-butyl-3-mercapto-1,2,4-triazin-5-one in 200 ml of 1 N sodium hydroxide solution at room temperature. The reaction mixture was stirred for approximately 20 hours at room temperature, the organic phase was then taken up in chloroform, and the solution was washed with three times 150 ml of 0.1 N sodium hydroxide solution, dried over sodium sulphate, filtered and concentrated. The oily residue was degassed at 50° C./0.05 mbar, and recrystallized from ethyl acetate/petroleum ether. 20.8 g (40% of theory) of 3-allylthio-4-amino-6-fluoro-tert.-butyl-1,2,4-triazin-5-one of melting point 75° to 74° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04470842
Source datasetuspto-grants-1984_09
ORD IDord-a65f8d25abe948d0b908879ad2187c82
Source noteuspto-grants-1984_09