HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-(2-Biphenylyl)-2-ethylpropionyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(2-Biphenylyl)-2-ethylpropionic acid | HCID 21571983 | — |
| Product | 3-(2-Biphenylyl)-2-ethylpropionyl chloride | HCID 22340217 | 106.3% |
Reaction Steps
To a 100-ml three-necked round flask (equipped with a stirrer tip, a Dimroth condenser, a thermometer and a trap of NaOH) were introduced 13.3 g (52.4 mmol) of 3-(2-biphenylyl)-2-ethylpropionic acid and 25.9 ml (355 mmol) of thionyl chloride, and they were refluxed for 2.5 hours with heating in a nitrogen atmosphere. After the reaction was completed, the unreacted thionyl chloride was distilled off under reduced pressure to obtain 15.2 g of a crude product as a yellow orange liquid. This acid chloride was used for the next reaction without further purification. The properties of the product thus obtained are described below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998039 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-e4cffc689b074805beb42db5135341c2 |
| Source note | uspto-grants-1999_12 |