HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886259Generated: October 25, 2026
Dimethylformamide → N-hydroxy-N-(1-hydroxy-2-naphthyl)-6-methoxycarbonylhexanamide
https://huagongshe.com/reaction/1886259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Methyl hydrogen heptane-1,7-dioate | HCID 88467 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 1-Hydroxy-2-naphthylhydroxylamine hydrochloride | HCID 85613850 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-hydroxy-N-(1-hydroxy-2-naphthyl)-6-methoxycarbonylhexanamide | HCID 15728702 | 78% |
Reaction Steps
Into a 25 ml methylene chloride solution of 500 mg (2.87 mmol) of 6-methoxycarbonylhexanoic acid and 222 μl (2.87 mmol) of DMF was added 564 μl (6.46 mmol) of oxalyl chloride at 0° C., and the mixture was stirred as such for one hour. The mixture was then added to a solution of 3.17 g (15 mmol) of 1-hydroxy-2-naphthylhydroxylamine hydrochloride, 3.1 ml (23 mmol) of triethylamine in THF (25 ml), and water (5 ml), at 0° C., and after stirring at 0° C. for one hour and at room temperature for one hour, the reaction was completed with aqueous KHSO4, and the mixture was extracted with methylene chloride. The organic layer was washed with 4N HCl and with saturated aqueous NaCl, and then dried over anhydrous magnesium sulfate, and after evaporation of the solvent under a reduced pressure, the residue was subjected to silica gel column chromatography to give 738 mg (78%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05149859 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-199c8b68f33746bbaca7158659228c2f |
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| Source note | uspto-grants-1992_09 |
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