HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4,5-Trimethoxyphenol → N-cyclohexyl-N-cyclopentyl-4-(3,4,5-trimethoxyphenoxy)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4,5-Trimethoxyphenol | HCID 69505 | — |
| Reactant | 4-bromo-N-cyclohexyl-N-cyclopentylbenzamide | HCID 19754888 | — |
| Solvent | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Product | N-cyclohexyl-N-cyclopentyl-4-(3,4,5-trimethoxyphenoxy)benzamide | HCID 19754874 | — |
Reaction Steps
The reaction and workup were carried out in the same manner as described in Example 1 using p-bromobenzoic acid N-cyclopentyl-N-cyclohexyl amide (2.285 g, 6.52 mmol), 3,4,5-trimethoxy phenol (1.199 g, 6.51 mmol) and cuprous oxide (486 mg, 3.40 mmol) in 2,4,6-collidine (15 ml). The crude product was chromatographed on silica gel using mixtures of ethyl acetate and hexane as eluents to give the title compound as a crystalline solid that could be recrystallized from ethyl acetate and hexane, m. pt. 166.16° C. (DSC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05223539 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-6c37a885d2aa46f6a3a27101f578bc32 |
| Source note | uspto-grants-1993_06 |