HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Methoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Benzyl-4-methoxybenzoic acid | HCID 22555978 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxybenzamide | HCID 76959 | — |
Reaction Steps
To a solution of 2-benzyl-4-methoxybenzoic acid (14.2 g) in 600 mL CH2Cl2 was added a catalytic amount of DMF, followed by a solution of oxalyl chloride (8.7 g) in 100 mL of CH2Cl2. The reaction was stirred at room temp overnight, then concentrated and azeotroped with toluene (2×). The residue was dissolved in 700 mL CH2Cl2 and cooled to 0 C. Tert-butyl amine (13.9 g) was added, and the reaction was warmed to room temp. After 1.5 h, the reaction was quenched with 5% aqueous KHSO4. The organic solution was separated, washed once with saturated aqueous sodium bicarbonate, dried (Na2SO4) and concentrated to give 15.9 g of 2-benzyl-N-tert-butyl)-4-methoxybenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723352B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-7b726dcc643e41839b95d12f44fe52b9 |
| Source note | uspto-grants-2010_05 |