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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288568Generated: October 31, 2026

p-Toluenesulfonyl azide → HCID 21938930, compound

https://huagongshe.com/reaction/2288568

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonyl azideHCID 13661—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18699519HCID 18699519—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 21938930HCID 21938930—

Reaction Steps

3.0 g of the cyclohexylsulfonyl-(4-methoxyphenylsulfonyl)methane prepared in (2), was put into a flask, and 100 mL of ethanol was added thereto, followed by stirring. Further, to this solution, 8.0 g of a 5 wt % ethanol solution of sodium hydroxide was added, followed by stirring. This reaction solution was cooled to from -5° C. to -10° C., and 35 mL of pure water was added thereto. Then, 10 mL of the ethanol solution containing 2.0 g of p-toluenesulfonylazide obtained in Reference Example 2, was dropwise added thereto over a period of 5 minutes, and the mixture was stirred for 3 hours and left to stand overnight. Then, the precipitate was collected by filtration to obtain crude crystals. The crude crystals were re-crystallized from ethanol to obtain cyclohexylsulfonyl-(4-methoxyphenylsulfonyl)diazomethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090518
Source datasetuspto-grants-2000_07
ORD IDord-cdd7f61155764e3eb4bdc7405af2b10f
Source noteuspto-grants-2000_07