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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608693Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 20087063, compound

https://huagongshe.com/reaction/1608693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 20087060HCID 20087060—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventBenzeneHCID 241—
ProductHCID 20087063HCID 20087063—

Reaction Steps

A solution of 60 g tosylchloride in 400 ml benzene is added to a stirred and cooled mixture of 17.5 g 2-cyanomethyl1,3 propanediol, 1.3 g triethylbenzylammonium chloride and 150 ml 30% (w/w) aqueous NaOH solution. This mixture is stirred overnight. The organic and aqueous layers are separated and the aqueous layer is washed with diethylether. The combined organic phase is washed with water until neutral, dried and evaporated. 2-Cyanomethyl-1,3-bis(tosyloxy)propane is obtained in a obtained in a yield of 62 g; liquid. Identification by means of IR, NMR and mass spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395946
Source datasetuspto-grants-1995_03
ORD IDord-3cf151e213a042c6bc8fa6bdedd605b0
Source noteuspto-grants-1995_03