Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178516123 | HCID 178516123 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178427632 | HCID 178427632 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05306600 |
|---|
| Source dataset | uspto-grants-1994_04 |
|---|
| ORD ID | ord-fbbeb606e327411a81e1cddc364d7059 |
|---|
| Source note | uspto-grants-1994_04 |
|---|