HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717464Generated: October 31, 2026
Triethylamine → 3-Chloro-5-difluoromethoxy-N-methoxy-N-methylbenzamide
https://huagongshe.com/reaction/1717464
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Chloro-5-(difluoromethoxy)benzoic acid | HCID 21904606 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chloro-5-difluoromethoxy-N-methoxy-N-methylbenzamide | HCID 21904658 | 93.8% |
Reaction Steps
3-Chloro-5-difluoromethoxybenzoic acid (1.8 g, 8 mmol; see step (iii) above) and oxalyl chloride (1.5 g, 11.8 mmol) were dissolved in methylene chloride (50 mL). DMF (2 drops) was added and the reaction mixture was stirred at ambient temperature for 30 minutes. Then, N,O-dimethylhydroxylamine (1 g, 10.2 mmol) and triethylamine (3 g, 30 mmol) were added and after another 10 minutes stirring at ambient temperature, the reaction mixture was concentrated at reduced pressure. The residue was taken up in ether (100 mL) and water (50 mL). After separation, the organic phase washed with brine, dried over sodium sulphate, filtered and concentrated. This residue was chromatographed on silica (hexane/ethyl acetate 2:1) which gave 2 g, 7.5 mmol (93%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803954B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-9186e66342b04e2a94289a508be26877 |
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| Source note | uspto-grants-2010_09 |
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