HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729847Generated: November 2, 2026
Methyl Methanesulfonate → N-Methylcaprolactam
https://huagongshe.com/reaction/1729847
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Methanesulfonate | HCID 4156 | — |
| Reactant | Caprolactam | HCID 7768 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-Methylcaprolactam | HCID 17369 | 88.85% |
Reaction Steps
A suspension of 8.42 g of 57% NaH-mineral oil (4.8 g, 0.2 mole of NaH) was washed with 2 × 400 ml portions of dry toluene (distilled from CaH2). After the washing was completed, 350 ml of dry toluene was added and the suspension mechanically stirred while a solution of 20 g (0.177 mole) of azacycloheptan-2-one in 50 ml of dry toluene was added dropwise over 1 hour. After the addition was completed, the mixture was refluxed with stirring for 1 hour, then cooled to 25° C and 22.0 g (0.2 mole) of methyl mesylate was added dropwise over 1 hour. After the addition was complete, the mixture was warmed with stirring to 50° for 1 hour. The mixture was cooled, filtered and the solid was resuspended in 100 ml toluene and filtered. The combined filtrates were concentrated and the residue was distilled at 85°-87°/0.1mm to yield 20 g (88.85%) of product. On 5% SE-30 column it showed one peak.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03989816 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-0b0aa960bae64f25a2e2cabdb1736bbb |
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| Source note | uspto-grants-1976_11 |
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