HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Heptyloxy)benzoyl chloride → 4-((4-Nitrobenzamido)methyl)phenyl 4-(heptyloxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Heptyloxy)benzoyl chloride | HCID 2724182 | — |
| Reactant | N-(4-hydroxybenzyl)-4-nitrobenzamide | HCID 12714523 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-((4-Nitrobenzamido)methyl)phenyl 4-(heptyloxy)benzoate | HCID 89253041 | 73% |
Reaction Steps
Prepared using General Procedure 2: To a stirring solution of N-(4-hydroxybenzyl)-4-nitrobenzamide INT-1 (647 mg, 2.38 mmol) in DCM (10 mL) at 0° C. was added TEA (1.03 mL, 7.13 mmol) followed by 4-(heptyloxy)benzoyl chloride (12.4 mL, 2.85 mmol). The suspension was sonicated until clear then diluted with DCM (50 mL) and washed with NaHCO3 (20 mL). The organic layer was concentrated and purified by chromatography (EA/hexanes) to provide 857 mg (73%) of 4-((4-nitrobenzamido)methyl)phenyl 4-(heptyloxy)benzoate INT-2. LCMS-ESI (m/z) calculated for C28H30N2O6: 490; found 491 [M+H]+, tR=3.41 min (Method 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278910B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-d14024c373c8414da7ec56315486a940 |
| Source note | uspto-grants-2016_03 |