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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911702Generated: November 1, 2026

Benzoyl Peroxide → HCID 66938894, compound

https://huagongshe.com/reaction/1911702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 86621227HCID 86621227—
SolventChloroformHCID 6212—
ProductHCID 66938894HCID 6693889474.1%

Reaction Steps

5-(2-Azidomethyl-4-chloro-phenyl)-1-trityl-1H-tetrazole: To 114A (4 g, 9.15 mmol) in chloroform (20 mL) was added NBS (1.711 g, 9.61 mmol) and benzoyl peroxide (30 mg, 0.124 mmol) and the reaction was heated at reflux overnight. Additional NBS and peroxide were added and the reaction was heated an addition 2 h. The reaction was cooled to rt, filtered, and purified by flash chromatography to give 5-(2-bromomethyl-4-chloro-phenyl)-1-trityl-1H-tetrazole (3.5 g, 74.1%). 1HNMR (400 MHz, CDCl3) δ: 4.78 (s, 2H), 7.04-7.14 (m, 5H), 7.24-7.35 (m, 11H), 7.40 (d, J=2.02 Hz, 1H), 8.06 (d, J=8.34 Hz, 1H). This intermediate (1.57 g, 3.04 mmol) and sodium azide (0.198 g, 3.04 mmol) in DMF (8 mL) were stirred for two days. The reaction was partitioned with EtOAc/water/brine and extracted with EtOAc. The combined organic layers were washed with water and brine, dried (MgSO4), and purified by flash chromatography to give 114B. LCMS m/z 195.2 (M+H−N3)+; 152.1 (M+H−N6)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604056B2
Source datasetuspto-grants-2013_12
ORD IDord-33fad7e9134f4ad2bf3b63579ccc1fa0
Source noteuspto-grants-2013_12