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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613525Generated: November 1, 2026

Diethyl Ether → HCID 178427632, compound

https://huagongshe.com/reaction/1613525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178516123HCID 178516123—
SolventTolueneHCID 1140—
ProductHCID 178427632HCID 178427632—

Reaction Conditions

Temperature40 °C

Reaction Steps

4.4 g (0.010 mol) of bis(cyclopentadienyl)bis(2,6-difluoro-3-hydroxyphenyl)titanium are suspended in 100 ml of toluene in a sulfation flask under nitrogen as protective gas. 5.7 g (0.030 mol) of toluene-4-sulfonyl chloride are then added. 30 ml of 1N sodiumhydroxide solution (0.030 mol) are then added dropwise. The reaction is slightly exothermic, and the temperature of the reaction mixture gradually increases to 40° C. The mixture is stirred for a further 3 hours while the temperature drops (thin-layer check of the reaction). 100 ml of ice-water and 100 ml of ether are then added. The organic phase is separated off and washed several times with a little water until the washings are neutral. The organic phase is dried using magnesium sulfate and evaporated on a vacuum rotary evaporator. An orange product remains which, after purification by chromatography on silica gel using toluene as eluent, gives orange crystals having a melting point of 185°-187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192642
Source datasetuspto-grants-1993_03
ORD IDord-6455e5b4698340b0b2495b5ef3a7c9ab
Source noteuspto-grants-1993_03