HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 67826442, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | 2-Methylbutanoic Acid | HCID 8314 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67826442 | HCID 67826442 | 99.1% |
Reaction Steps
5.49 g of (+)-2-methylbutanoic acid,8.50 g of 4-hydroxy biphenyl and 20 ml of toluene were charged into a flask and then 4.0 ml (55 mmol) of thionyl chloride was added thereto with stirring. The resulting mixture was maintained at a temperature of 70°~80° C. and reacted for 8 hours. After the completion of the reaction, the resulting product was cooled to room temperature, added with water to decompose the excess amount of thionyl chloride, washed with water and dried on anhydrous magnesium sulfate. After the removal of solvent, it was purified by a column chromatography of silica gel to obtain 12.69 g of (+)-2-methylbutanoic acid biphenyl having an oily specific rotation [α]25 (16.46 wt% in chloroform) of +15.1°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05137653 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-50eb68cea4e14c11b4663cb90ac08145 |
| Source note | uspto-grants-1992_08 |