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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627356Generated: November 1, 2026

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

https://huagongshe.com/reaction/1627356

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 numberUS08785488B2
Source datasetuspto-grants-2014_07
ORD IDord-c0852287ce9c47198c7a97d15255b39f
Source noteuspto-grants-2014_07