HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467475Generated: October 29, 2026
Methanesulfonic Acid → 7-Methylcaprolactam
https://huagongshe.com/reaction/467475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2-Methylcyclohexanone | HCID 11419 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 7-Methylcaprolactam | HCID 137273 | — |
Reaction Steps
Methanesulfonic acid (15 mL) was added to a solution of 2-methylcyclohexanone (2-1, 6.00 g, 53.5 mmol, 1 equiv) in DME (20 mL) at −40° C. Sodium azide (8.69 g, 134 mmol, 2.50 equiv) was added in four equal portions over 1 h as cooling was maintained. The cold bath was then removed and the reaction mixture was warmed to 23° C. and stirred for 20 h. The mixture was diluted with DME (20 mL) and basified to pH 9 with concentrated aqueous ammonium hydroxide solution. The resulting mixture was partitioned between brine (200 mL) and ethyl actetate (4×200 mL). The combined organic layers were dried over sodium sulfate and concentrated to give 7-methylazepan-2-one (2-2) as a pasty white solid. 1H NMR (300 MHz, CDCl3) δ 5.50 (br s, 1H), 3.50 (m, 1H), 2.43 (m, 2H), 2.05-1.30 (m, 6H), 1.21 (d, 3H,J=7.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08623863B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-47cf7eae5da54c949c23f398c0661552 |
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| Source note | uspto-grants-2014_01 |
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