HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72592Generated: October 25, 2026
Benzyl Bromide → 4-benzyl-6-bromo-spiro[3H-1,4-benzoxazine-2,1-cyclopropane]
https://huagongshe.com/reaction/72592
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromo-3,4-dihydrospiro[benzo[b][1,4]oxazine-2,1'-cyclopropane] | HCID 58340860 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-benzyl-6-bromo-spiro[3H-1,4-benzoxazine-2,1-cyclopropane] | HCID 58340778 | 26.5% |
Reaction Steps
To a stirred solution of 6-bromospiro[3,4-dihydro-1,4-benzoxazine-2,1′-cyclopropane] (3.11 g, 12.9 mmol) in DMF (20 mL) was added potassium carbonate (3.6 g, 26.0 mmol) and benzyl bromide (1.61 mL, 13.6 mmol). The reaction mixture was heated at 60° C. for 6 h then cooled to room temperature and quenched by the addition of water. The reaction mixture was extracted with ethylacetate (2×50 mL) and the combined organic layers were washed with water (20 mL) and brine (20 mL), then dried over sodium sulfate, filtered and concentrated. The crude product was purified by silica gel column chromatography to furnish 4-benzyl-6-bromo-spiro[3H-1,4-benzoxazine-2,1′-cyclopropane] (1.13 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828951B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-612f7ee0699e48ccb5b343cb448e333b |
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| Source note | uspto-grants-2014_09 |
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