HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 86756730, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 86756731 | HCID 86756731 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86756730 | HCID 86756730 | 55.7% |
Reaction Steps
A solution of 0.32 g of (E)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-isobutryl-2′-isobutyl-4-methylvalerohydrazide in 10 ml of methanol was treated with 0.03 g of 4-toluenesulphonic acid. The mixture was stirred for 2 hours at room temperature and then the solvent was evaporated to leave a glass. This residue was triturated with diethyl ether to give 0.15 g of (E)-2(R)-[1(S)-(hydroxycarbamoyl)-4-phenyl-3-butenyl]-2′-isobutyryl-2′-isobutyl-4-methylvalerohydrazide in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06235787B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-c9dcee4c77914b819d8649e717797eb2 |
| Source note | uspto-grants-2001_05 |