HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440156Generated: October 26, 2026
Sulfuric Acid → 2-Propenoic acid, 3-(4-methoxyphenyl)-, 2-ethylhexyl ester
https://huagongshe.com/reaction/440156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Ethylhexyl acrylate | HCID 7636 | — |
| Reactant | 2-Ethylhexanol | HCID 7720 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Pentyl nitrite | HCID 10026 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Propenoic acid, 3-(4-methoxyphenyl)-, 2-ethylhexyl ester | HCID 21630 | — |
Reaction Steps
12.3 g of 4-anisidine (4-methoxyaniline) are mixed with stirring with 10 ml of concentrated sulfuric acid and 60 ml of 2-ethylhexanol and the mixture is cooled to about 10° C. 11.7 g of amyl nitrite are then slowly added and the mixture is stirred for a further 40 minutes after addition is completed. 20.2 g of 2-ethylhexyl acrylate and 100 mg of Pd (5% by weight of Pd on activated charcoal) are then added to the reaction mixture which is heated in the course of 1 hour to 65° C. and stirred for 12 hours at this temperature. The mixture is diluted with 100 ml of water and extracted with 200 ml of dichloromethane. As studies by thin-layer chromatography and gas chromatography show, 2-ethylhexyl p-methoxycinnamate has not formed even in the smallest amounts. The 2-ethylhexyl acrylate used is present essentially in unchanged form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05516932 |
|---|
| Source dataset | uspto-grants-1996_05 |
|---|
| ORD ID | ord-7bfe1daee73a4841b532e7b6e837d8c6 |
|---|
| Source note | uspto-grants-1996_05 |
|---|