HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81166Generated: October 31, 2026
Potassium tert-butoxide → trans-4-benzyltetrahydro-2H-furo[3,4-b][1,4]oxazin-3(4H)-one
https://huagongshe.com/reaction/81166
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | trans-N-benzyl-2-chloro-N-(4-hydroxytetrahydrofuran-3-yl)acetamide | HCID 86724520 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | trans-4-benzyltetrahydro-2H-furo[3,4-b][1,4]oxazin-3(4H)-one | HCID 86724521 | — |
Reaction Steps
To a solution of trans-N-benzyl-2-chloro-N-(4-hydroxytetrahydrofuran-3-yl)acetamide (4.7 g, 17.4 mmol) in t-BuOH (40 mL) was added KOt-Bu (1.0 M in THF; 34.8 mL, 34.8 mmol) solution at 25° C. The reaction mixture was stirred at 25° C. for 2 hours and then the solvent was evaporated under reduced pressure. The residue was dissolved in water and extracted with EtOAc (100 mL). The organic extract was washed with brine (40 mL), dried over anhydrous Na2SO4, and concentrated under reduced pressure to afford trans-4-benzyltetrahydro-2H-furo[3,4-b][1,4]oxazin-3(4H)-one. MS APCl calc'd for C13H15NO3 [M+H]+ 234. found 234.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846657B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a7150dc860d6473587c5561b02fc8374 |
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| Source note | uspto-grants-2014_09 |
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