HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → 2-Methyl-5-(5-methyl-[1,3,4]oxadiazol-2-yl)-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Triethyl orthoacetate | HCID 66221 | — |
| Reactant | 3-HYDROXY-4-METHYLBENZOIC ACID ETHYL ESTER | HCID 15745489 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-Methyl-5-(5-methyl-[1,3,4]oxadiazol-2-yl)-phenol | HCID 59649721 | — |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
A suspension of ethyl 3-hydroxy-4-methylbenzoate (3.60 g, 20 mmol) in anhydrous hydrazine (10 mL, 318 mmol) (Aldrich) was heated at reflux (150° C. bath temperature) for 3 hours. After cooling to room temperature, the mixture was concentrated under reduced pressure to give a dry solid. This was suspended in xylene (50 mL) and concentrated under reduced pressure. The resulting solid was suspended in triethyl ortho-acetate (35 mL, 191 mmol) (Aldrich) and heated at reflux (150° C. bath temperature) for 20 hours with removal of ethanol. After cooling, dichloromethane was added and the solid was collected by filtration to give 2-methyl-5-(5-methyl-[1,3,4]oxadiazol-2-yl)-phenol as an off-white crystalline material. (Yield 2.28 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07968554B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-2ed7546fa3f849f19241c453cd7825a8 |
| Source note | uspto-grants-2011_06 |