HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 178506636, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | HCID 19103907 | HCID 19103907 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178506636 | HCID 178506636 | — |
Reaction Steps
A solution of 7 g of 1-(4-t-butylphenyl)cyclopent-2-en-1-ol (0.032 mole) and 0.1 g of p-toluenesulphonic acid (0.00058 mole) in 70 ml toluene was gently heated to 40° C. for 5 minutes. The mixture was washed with aqueous sodium hydroxide and subsequently with water. After drying the organic phase over magnesium sulphate for 2 hours, 20.3 ml of a solution of n-butyllithium in hexane (1.6 mole/liter, 0.032 mole n-butyllithium) was added. A precipitate was formed and the precipitate was washed three times with hexane to obtain 4-t-butylphenylcyclopentadienyllithium as an off-white solid material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05279999 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-3d7c06b439d04c1cb85910e249907bab |
| Source note | uspto-grants-1994_01 |