HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196380Generated: October 31, 2026
o-Benzylbenzoic acid → 2-benzyl-N-methylbenzamide
https://huagongshe.com/reaction/2196380
Participants
| Role | Name | HCID | Charge |
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| Reactant | o-Benzylbenzoic acid | HCID 11924 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-benzyl-N-methylbenzamide | HCID 4128509 | 44,856.801% |
Reaction Steps
To a stirred solution of α-phenyl-o-toluic acid (2.0 g, 9.43 mmol) in methylene chloride (500 mL) at room temperature under argon was added by dropwise addition a solution of oxalyl chloride (0.988 mL, 11.3 mmol) in methylene chloride (50 mL). N,N-Dimethylformamide (10 drops) were added and the contents of the reaction flask were stirred 1.5 h. Solvent was removed in vacuo and methylene chloride (100 mL) and methylamine hydrochloride (950 mg, 14.1 mmol) was added. With ice-bath cooling a solution of N,N-diisopropylethylamine (4.10 mL, 23.6 mmol) in methylene chloride (10 mL) was added dropwise. Saturated sodium bicarbonate was added and the resulting mixture extracted with methylene chloride (3×). The combined organic extracts were dried with sodium sulfate (anh.). Filtration followed by removal of the solvent in vacuo gave a solid which after trituration with ether afforded N-Methyl-2-(phenylmethyl)benzamide (974 mg, 4.23 mol, 46%). MS [M+H]+ 226
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338449B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-4e051715dadc4ef7b90058ce0d540bb4 |
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| Source note | uspto-grants-2012_12 |
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