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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820257Generated: November 2, 2026

Trimethylsilyldiazomethane → Methyl 5-bromo-2-tert-butylpyrimidine-4-carboxylate

https://huagongshe.com/reaction/1820257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant5-Bromo-2-(tert-butyl)pyrimidine-4-carboxylic acidHCID 12258914—
SolventBenzene methanolHCID 21927730—
ProductMethyl 5-bromo-2-tert-butylpyrimidine-4-carboxylateHCID 5788883581%

Reaction Steps

A 2.0 M hexanes solution of trimethylsilyldiazomethane (11.8 mL, 23.62 mmol) was added dropwise to a stirring solution of 5-bromo-2-tert-butyl-pyrimidine-4-carboxylic acid (6.12 g, 23.62 mmol) in 9:1 benzene/methanol (100 mL), and the reaction was stirred for 2 days. TLC analysis showed that the reaction was complete, so the mixture was concentrated in-vacuo. The residue was dissolved in ethyl acetate (100 mL), washed with water (3×20 mL), dried over sodium sulfate, then concentrated in-vacuo. Purified over silica gel, eluting with 10% ethyl acetate/hexanes, to yield 5.2 g of a colorless oil as product. MS (ESI+)=273/275, (M+H)+. Yield=81%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601844B2
Source datasetuspto-grants-2009_10
ORD IDord-9638925f7478451981cfe1e745b9f120
Source noteuspto-grants-2009_10