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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258812Generated: November 1, 2026

Benzyl Bromide → HCID 58340852, compound

https://huagongshe.com/reaction/1258812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67115789HCID 67115789—
SolventDimethylformamideHCID 6228—
ProductHCID 58340852HCID 5834085269%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 6-(5-bromo-2-chloro-benzyl)-3,4-dihydro-2H-benzo[1,4]oxazine (8.0 g, 23.66 mmol) in DMF (35 mL) was added potassium carbonate (6.53 g, 36.0 mmol), benzyl bromide (4.33 mL, 35.50 mmol) and heated to 50° C. for 8 h. Reaction mixture was cooled to room temperature, quenched by the addition of water (50 mL), extracted with ethyl acetate (3×20 mL). The organic layer was washed with water (50 mL), brine (50 mL), dried over sodium sulfate, concentrated and purified by silica gel column chromatography to furnish 4-benzyl-6-(5-bromo-2-chloro-benzyl)-3,4-dihydro-2H-benzo[1,4]oxazine (7.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466114B2
Source datasetuspto-grants-2013_06
ORD IDord-c5d15fb6dcfa4c1c99bc3eb458a95f5a
Source noteuspto-grants-2013_06