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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866935Generated: October 31, 2026

Benzoyl Peroxide → tert-butyl 4-(bromomethyl)-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/1866935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 23021524HCID 23021524—
SolventCarbon TetrachlorideHCID 5943—
Producttert-butyl 4-(bromomethyl)-1H-pyrazole-1-carboxylateHCID 5806667230%

Reaction Steps

To a solution of 4-methylpyrazole-1-carboxylic acid tert-butyl ester (1.0 g, 5.5 mmol) in carbon tetrachloride (20 mL) was added N-bromosuccinimide (1.0 g, 5.6 mmol) and benzoyl peroxide (50 mg), and the reaction mixture was heated at reflux for 16 h. The reaction mixture was cooled to room temperature, filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:4 EtOAc/hexanes) provided 4-bromomethylpyrazole-1-carboxylic acid tert-butyl ester as a light yellow oil (0.42 g, 30%): 1NMR (300 MHz, CDCl3) δ 8.10 (s, 1H), 7.74 (s, 1H), 4.39 (s, 2H), 1.65 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629363B2
Source datasetuspto-grants-2009_12
ORD IDord-2decb5bab9d5478da2ea452ebffc94dc
Source noteuspto-grants-2009_12