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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912354Generated: November 4, 2026

Bromine → 5-Benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1912354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant5-benzoyl-1,3,6-trimethyl-2,4(1H,3H)-PyrimidinedioneHCID 802308—
SolventChloroformHCID 6212—
Product5-Benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dioneHCID 95031957.6%

Reaction Steps

(See, e.g., Tsupak et al., Khimiya Geterotsiklicheskikh Soedinenii. 7:1096-1102 (2003); Tsupak et al., Russ. Chem. Bull. 55:2265-2270 (2006)). To a solution of 3 (2.61 g, 10.1 mmol) in chloroform (13 mL) was added bromine (1.62 g, 0.52 mL, 20.3 mmol in 3 mL chloroform) dropwise over 30 min at room temperature. The reaction mixture was further stirred for 1 min at room temperature before concentrated in vacuo. The crude reaction mixture was purified by flash chromatography to yield 4 (1.96 g, 57%); mp 164-167° C.; MS (ES+) (m/z): [M+1]+ calculated for C14H14BrN2O3, 338.18. found 337.15, 338.93. This compound matched analytical data as reported (see, e.g., Tsupak et al., Khimiya Geterotsiklicheskikh Soedinenii., supra; Tsupak et al., Russ. Chem. Bull., supra).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609661B2
Source datasetuspto-grants-2013_12
ORD IDord-d9cfd0e3aeaa46eda34828f4e69f3f7b
Source noteuspto-grants-2013_12