HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]propanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-[3,3-Bis(ethyloxy)propyl]-5-(phenylmethyl)-1,2,4-oxadiazole | HCID 66812952 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[5-(Phenylmethyl)-1,2,4-oxadiazol-3-yl]propanal | HCID 86643113 | 89.9% |
Reaction Steps
Crude 3-[3,3-bis(ethyloxy)propyl]-5-(phenylmethyl)-1,2,4-oxadiazole (5.63 g, 19.4 mmol) in EtOH (75 ml) was stirred with p-toluenesulphonic acid (0.738 g, 3.9 mmol) for 21 h and the mixture partitioned between EtOAc and water. The organics were isolated washed with water and brine, dried and concentrated to a red oil. This material contained significant amounts of acetal, therefore the oil was dissolved in THF (15 ml) and treated with 2M HCl solution for 2 h then partitioned between EtOAc and water. The organics were isolated washed with brine, dried and concentrated to yield 3-[5-(phenylmethyl)-1,2,4-oxadiazol-3-yl]propanal as a red/brown oil (3.77 g) which was used crude in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143264B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-0cd3cb331f5641daa9cc2fb8ba8eadb5 |
| Source note | uspto-grants-2012_03 |