HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222341Generated: October 30, 2026
Dimethylformamide → 3-Hydroxy-2-methylbenzamide
https://huagongshe.com/reaction/222341
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Hydroxy-2-methylbenzoic Acid | HCID 252023 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Hydroxy-2-methylbenzamide | HCID 19082098 | 45% |
Reaction Steps
Oxalyl chloride (4.19 ml, 48 mmol) was added to an ice-cold solution of 3-hydroxy-2-methylbenzoic acid (3.62 g, 24 mmol) in dichloromethane (30 mL). N,N-dimethylformamide (2 mL) was then added and the mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo and the residue was concentrated in vacuo three times from toluene. The residue was then suspended in tetrahydrofuran (10 mL), added to ice-cold 0.88 ammonia solution (10 mL) and stirred for 2.5 hours, allowing the temperature to rise to ambient. The reaction mixture was then extracted with ethyl acetate, dried over magnesium sulfate and concentrated in vacuo and the residue was concentrated in vacuo from acetone and triturated with diethyl ether to afford the title compound as a solid in 45% yield. LRMS APCI m/z 152 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207198B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-16c1b11d3e9749b294f3286c851f3794 |
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| Source note | uspto-grants-2012_06 |
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