HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730810Generated: October 25, 2026
Water → N-cyclohexyl-2,4,5-trimethylfuran-3-hydroxamic acid
https://huagongshe.com/reaction/1730810
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-Cyclohexylhydroxylamine hydrochloride | HCID 3084432 | — |
| Reactant | 2,4,5-Trimethyl-3-furancarbonyl chloride | HCID 14535934 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cyclohexyl-2,4,5-trimethylfuran-3-hydroxamic acid | HCID 21496536 | — |
Reaction Steps
49 Parts of N-cyclohexylhydroxylamine hydrochloride is dissolved in 400 parts of dichloromethane; at room temperature a solution of 50.4 parts of sodium hydrogen carbonate in 500 parts of water and subsequently 51.6 parts of 2,4,5-trimethylfuran- 3-carboxylic chloride are added to the mixture. After the mixture has been stirred for 2 hours the dichloromethane phase is separated, dried over anhydrous sodium sulfate and evaporated. There is obtained 75 parts of N-cyclohexyl-2,4,5-trimethylfuran-3-hydroxamic acid in the form of an oil. This oil is dissolved in 300 parts of dichloromethane. To this solution there is added 36 parts of sodium hydroxide in 200 parts of water and 75.6 parts of dimethyl sulfate and the whole is stirred for 2 hours. The dichloromethane phase is then separated, washed with water until neutral, dried over anhydrous sodium sulfate and evaporated. Upon distillation of the residue there is obtained 52 parts of O-methyl-N-cyclohexyl-2,4,5-trimethylfuran-3-hydroxamic acid having a boiling point at 0.3 mm Hg of 128° to 130° C and the refractive index nD25 : 1.5021. ##SPC11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03993772 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-69d4ab0d52e04d5394e67c84a103ebd5 |
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| Source note | uspto-grants-1976_11 |
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