HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073474Generated: November 1, 2026
Hydrochloric Acid → (+)-4-(2-Methyloctanoyl) biphenyl 2-methyloctanoate
https://huagongshe.com/reaction/1073474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-Methyl octanoic acid chloride | HCID 12812232 | — |
| Reactant | (+)-Biphenyl 2-methyloctanoate biphenyl | HCID 131716695 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | (+)-4-(2-Methyloctanoyl) biphenyl 2-methyloctanoate | HCID 131716694 | 49% |
Reaction Steps
Next, 2.02 g (11.4 mmol) of the above (+)-2-methyl octanoyl chloride and 3 ml of nitrobenzene were cooled to 0° C. in a flask and added with 3.06 g (22.9 mmol) of anhydrous aluminum chloride with stirring, which were stirred at room temperature for 30 minutes. Thereafter, 2.89 g (7 mmol) of (+)-biphenyl-2-methyloctanoate biphenyl dissolved in 3 ml of nitrobenzene was added thereto, which was reacted by stirring at room temperature for 140 hours. After the completion of the reaction, 2 normal hydrochloric acid and ice were added and extracted with chloroform. The extract was washed with water, dried on anhydrous magnesium sulfate and distilled to remove the solvent. The residue was purified through a column chromatography of silica gel to obtain 1.55 g (yield: 49%) of an oily (+)-4-(2-methyloctanoyl) biphenyl-2-methyloctanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04970023 |
|---|
| Source dataset | uspto-grants-1990_11 |
|---|
| ORD ID | ord-ab71cc87a6e14ab1b29f7fed5de0cda3 |
|---|
| Source note | uspto-grants-1990_11 |
|---|