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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-3,4-dihydrospiro[benzo[b][1,4]oxazine-2,1'-cyclopropane]HCID 58340860—
SolventDimethylformamideHCID 6228—
Product4-benzyl-6-bromo-spiro[3H-1,4-benzoxazine-2,1-cyclopropane]HCID 5834077826.5%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828951B2
Source datasetuspto-grants-2014_09
ORD IDord-612f7ee0699e48ccb5b343cb448e333b
Source noteuspto-grants-2014_09