HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058974Generated: October 25, 2026
2,3-Dimethylphenol → HCID 13192288, compound
https://huagongshe.com/reaction/2058974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dimethylphenol | HCID 10687 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-methanesulphonyl-hexahydro-4,5-epoxy-1H-azepine | HCID 20548908 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13192288 | HCID 13192288 | — |
Reaction Steps
7.0 g (0.036 mol) of 1-methanesulphonyl-hexahydro-4,5-epoxy-1H-azepine are dissolved, together with 8.9 g (0.073 mol) of 2,3-dimethyl-phenol, with 36.6 ml of 2 N sodium hydroxide solution (0.013 mol) in 200 ml of acetonitrile. The reaction mixture is heated under reflux for 5 days, then cooled to room temperature and concentrated under a water pump vacuum. The residue is then dissolved in 200 ml of methylene chloride and the organic phase is washed with three times 100 ml of 2 N sodium hydroxide solution and then with water, dried over sodium sulphate and evaporated under a water pump vacuum. The resulting crude product is purified by preparative thick layer chromatography (100×20 cm silica gel plates, layer thickness 1.5 mm). Crystalline trans-4-hydroxy-5-(2,3-dimethylphenoxy)-1-methanesulphonyl-hexahydro-1H-azepine with a melting point of 112°-115° is obtained by elution with a 3:1 mixture of toluene/ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04320137 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-7dcbefb13ab349adb2199ebd7a39a829 |
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| Source note | uspto-grants-1982_03 |
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