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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397152Generated: October 28, 2026

Water → n,n-Diphenyl-3-hydroxyimino-2-methyl-4-methylsulfonylbenzamide

https://huagongshe.com/reaction/397152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantButyl nitriteHCID 10996—
ReactantHCID 18757278HCID 18757278—
ReactantPotassium tert-butoxideHCID 23665647—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
Productn,n-Diphenyl-3-hydroxyimino-2-methyl-4-methylsulfonylbenzamideHCID 86654807—

Reaction Steps

A solution of 0.7 g (6.9 mmol) of n-butyl nitrite (97%) and 2 g (5.3 mmol) of N,N-diphenyl-2,3-dimethyl-4-methylsulfonyl-benzamide in 30 ml of dimethylformamide is cooled to from −55 to −60° C., and a solution of 1.4 g (12 mmol) of potassium tert-butoxide in 10 ml of dimethylformamide is added dropwise at this temperature, over a period of 20 minutes. The reaction is monitored by HPLC. For work-up, initially 10 ml of water are added, and the mixture is then adjusted to pH 5-6 using glacial acetic acid. The mixture is then poured onto 100 ml of ice-water and the aqueous phase is extracted with ethyl acetate. The organic phase is washed with sodium bicarbonate solution, dried over magnesium sulfate and concentrated. This gives 3.0 g of a partially crystalline crude product, which is purified by silica gel chromatography using the mobile phase toluene/acetone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608209B2
Source datasetuspto-grants-2003_08
ORD IDord-82bc6b93d3d94bc3aa94be8e261335c6
Source noteuspto-grants-2003_08