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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231578Generated: November 1, 2026

Methyl p-toluenesulfonate → HCID 13881298, compound

https://huagongshe.com/reaction/231578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantSodium hydrideHCID 24758—
ReactantSodiumHCID 5360545—
ReactantHCID 13881297HCID 13881297—
SolventDimethylformamideHCID 6228—
SolventButyl ChlorideHCID 8005—
SolventEthyl AcetateHCID 8857—
ProductHCID 13881298HCID 13881298—

Reaction Steps

A solution of N,N-Dimethyl-2-[N-(2-hydroxyethyl)aminosulfonyl]-6-nitrobenzamide (3.97 g, 12.5 mmol) in dry DMF (40 ml) was added slowly to a stirred suspension of 50% NaH (0.60 g, 12.5 mmol) in dry DMF (10 ml) under N2 at 20-25°. After formation of the sodium salt was complete, a solution of methyl p-toluenesulfonate (2.40 g, 12.9 mmol) in DMF (4 ml) was added and the reaction mixture stirred at 20-25° for 20 hours and then at 60° for 23 hours. The orange solution was mixed with EtOAc (400 ml) and the white solid which formed was filtered off. This precipitate was washed with EtOAc (100 ml). The combined EtOAc solutions were washed with a saturated aqueous NaCl solution, dried (Na2SO4), filtered and concentrated under reduced pressure. Pure produced, mp 107-08°, 2.5 g (60%) was obtained by flash chromatography over silica gel and elution with a 65% n-butylchloride-35% acetonitrile solvent mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847294
Source datasetuspto-grants-1989_07
ORD IDord-0c88ae8ceca3423ca47c4bce13a30d22
Source noteuspto-grants-1989_07