HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 53651857, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | N-(p-Bromobenzyl)-N-(4-methoxyphenyl)hydrazine hydrochloride | HCID 19041688 | — |
| Reactant | HCID 54169137 | HCID 54169137 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53651857 | HCID 53651857 | — |
Reaction Steps
A mixture of ketone from Step 3 (92 mg, 0.3 mmol), N-(4-bromobenzyl)-N-(4-methoxyphenyl))hydrazine (52 mg, 0.3 mmol) from Example 1, Step 5, acetic acid (36 mg, 0.6 mmol) and toluene (3 mL) was stirred at room temperature for 1.5 h. The solvent was evaporated and replaced by ethanol (3 mL). Then acetyl chloride (110 mg, 5 eq) was added and the mixture was heated at 60° C. for 45 min. After evaporation of the ethanol, the mixture was chromatographed on silica gel, eluting with a 1:3 mixture of EtOAc and hexane, to afford the product as an oil which solidified (80 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05639780 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-4d662660a8df4417b12a9d9730731e4a |
| Source note | uspto-grants-1997_06 |