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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83871Generated: October 29, 2026

Sodium Azide → 4-(4-Azido-2-methyl-3-oxobutan-2-yl)-2-chlorobenzenesulfonamide

https://huagongshe.com/reaction/83871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantHCID 86662251HCID 86662251—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(4-Azido-2-methyl-3-oxobutan-2-yl)-2-chlorobenzenesulfonamideHCID 8666225079.4%

Reaction Steps

To a solution of 4-(4-bromo-2-methyl-3-oxobutan-2-yl)-2-chlorobenzenesulfonamide (11.3 g, 31.8 mmol) in DMF (50 mL) was added NaN3 (3.1 g, 47.8 mmol, 1.5 eq) at 0° C. After stirring 2 h, the residue was diluted with water and extracted with EtOAc. The combined extracts were washed with 1M HCl and water successively, dried over MgSO4, filtered and evaporated. The residue was purified by chromatography (Hex/EtOAc=4:1 to 2:1) to give 4-(4-azido-2-methyl-3-oxobutan-2-yl)-2-chlorobenzenesulfonamide (8.0 g, 79% yield) as yellow sticky oil. 1H NMR (400 MHz, CDCl3) δ 8.11 (d, J=8.4 Hz, 1H), 7.43 (s, 1H), 7.29 (d, J=2.2 Hz, 1H), 5.12 (s, 2H), 4.11 (s, 2H), 1.58 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846739B2
Source datasetuspto-grants-2014_09
ORD IDord-1fac26c6380f4ce8a6aa943fe5572fc2
Source noteuspto-grants-2014_09