HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637555Generated: October 30, 2026
Ethylene Glycol → 3-(2,4-Dimethoxyphenyl)octanoic acid
https://huagongshe.com/reaction/1637555
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (-)-2-(2,4-Dimethoxyphenyl)heptyl cyanide | HCID 19348443 | — |
| Product | 3-(2,4-Dimethoxyphenyl)octanoic acid | HCID 19348619 | 87% |
Reaction Steps
1.00 g (17.8 mmol) of potassium hydroxide was added to a solution of 1.27 g (4.86 mmol) of (-)-2-(2,4-dimethoxyphenyl)heptyl cyanide [prepared as described in step (ii) above] in 6 ml of ethylene glycol, and the resulting mixture was heated under reflux for 2.5 hours in an atmosphere of nitrogen. At the end of this time, the reaction mixture was cooled to room temperature, after which it was acidified with 1 N aqueous hydrochloric acid and then extracted with diethyl ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, after which the solvent was removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through 100 g of silica gel, using a 1:2 by volume mixture of ethyl acetate and hexane as the eluent, to give 1.19 g (yield 87%) of the title compound as crystals, melting at 51-52° C. (from pentane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06040339 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-73a4d36e8a90451f9ffa8102d8cd1765 |
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| Source note | uspto-grants-2000_03 |
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