HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 69292549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Diisopropanolamine | HCID 8086 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | 2-Ethylhexyl cyanoacetate | HCID 96359 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69292549 | HCID 69292549 | — |
Reaction Steps
A 250 ml three necked reaction flask, equipped with a reflux condenser combined with a water separator and an oil bath with a magnetic stirrer was charged with 3.8 g (25 mmol) of 4-carboxy-benzaldehyde (Fluka), 6.8 g (33 mmol) of cyanacetic-acid-2-ethyl-hexylester, 0.3 g of bis-(2-hydroxypropyl)-amine and 0.25 g of p-toluene-sulfonic acid in 80 ml of toluene and 20 ml of dimethylformamide. After 22 hours under reflux the reaction mixture was diluted with toluene and washed with aqueous NH4Cl and NaCl solutions, dried with Na2SO4 and concentrated to yield 6.2 g (74%) of whire crystals. M.p. 159-162° C. W(CH2C2) 305 nm (E=811).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414138B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-95517ed9513a40df9bb876998062206a |
| Source note | uspto-grants-2008_08 |