HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37119Generated: October 25, 2026
6-Oxabicyclo[3.1.0]hexane → 6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazine
https://huagongshe.com/reaction/37119
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-Oxabicyclo[3.1.0]hexane | HCID 9244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine | HCID 10535622 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-cyano-3,4-dihydro-2,2-dimethyl-4-(2-hydroxycyclopentan-1-yl)-2H-1,4-benzoxazine | HCID 19934564 | — |
Reaction Steps
In 20 ml of N,N-dimethylformamide was dissolved 1.0 g of 6-cyano-3,4-dihydro-2,2-dimethyl-2H-1,4-benzoxazine followed by addition of 0.24 g of sodium hydride. The mixture was stirred at 70° C. for 1 hour and after cooling to room temperature, 0.5 ml of cyclopentene oxide was added. The mixture was stirred at 70° C. for 3 hours. The reaction mixture was then allowed to cool, diluted with water and extracted with ethyl acetate. The extract was washed with water and aqueous sodium chloride solution and dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography and the resulting crude crystals were recrystallized from ethyl acetate-hexane to give 0.53 g of 6-cyano-3,4-dihydro-4-(2-hydroxycyclopentan-1-yl)-2,2-dimethyl-2H-1,4-benzoxazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420126 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-658be5a07e2c441eb1bd87c04cd5b359 |
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| Source note | uspto-grants-1995_05 |
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