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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184512Generated: October 31, 2026

Boron tribromide → 8-Hydroxy-2-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carbaldehyde

https://huagongshe.com/reaction/1184512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant8-Methoxy-2-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carbaldehydeHCID 82154055—
SolventDichloromethaneHCID 6344—
Product8-Hydroxy-2-methyl-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazine-6-carbaldehydeHCID 8666422577%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a 200 mL round-bottomed flask cooled in an ice/brine bath was added BBr3 (3.4 g, 13.56 mmol) in DCM (30 mL) under N2. A solution of 17 in DCM (10 mL) was added drop-wise to the cooled BBr3 solution. The reaction was stirred under N2 for 1 hr, then allowed to warm to 23° C. After 2 hr, the reaction was poured over ice and the resulting solid was isolated by vacuum filtration, washed with water, and dried in vacuo to give a tan solid (0.722 g, 77% yield): 1H NMR (400 MHz, DMSO-d6) δ ppm 1.40-1.50 (m, 3H) 4.76 (q, J=6.74 Hz, 1H) 6.93 (d, J=2.02 Hz, 1H) 7.04 (d, J=2.02 Hz, 1H) 9.72-9.77 (m, 1H) 9.95-10.01 (m, 1H) 10.85 (s, 1H). ESI-MS: m/z 208.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669249B2
Source datasetuspto-grants-2014_03
ORD IDord-d3ba603faa9f45e28a413eb6313bb9d5
Source noteuspto-grants-2014_03