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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461696Generated: October 29, 2026

Benzyl Bromide → HCID 15056724, compound

https://huagongshe.com/reaction/1461696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 15056723HCID 15056723—
ProductHCID 15056724HCID 1505672462.3%

Reaction Steps

7.7 g (45 mmol) of benzyl bromide are added dropwise at room temperature to a solution of 10 g (46.9 mmol) of 1-tert.-butyl-3-ethyl-1,3,5-triazine-2,4,6-trione and 9.9 g (93 mmol) of sodium carbonate. The reaction mixture is refluxed for 6 hours. After it has cooled, the solid constituents are separated off, and the reaction solution is concentrated. The residue is taken up in methylene chloride and washed twice with water. After the organic phase has been dried over sodium sulphate, it is concentrated and distilled in vacuo. 8.5 g (60% of theory) of 5-benzyl-1-tert.-butyl-3-ethyl-1,3,5-triazine-2,4,6-trione are obtained as a highly viscous oil having a boiling point of 170° C./0.03 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05077291
Source datasetuspto-grants-1991_12
ORD IDord-5667decd4cd643b48c902fbcd83bee73
Source noteuspto-grants-1991_12