Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585459Generated: October 29, 2026

1-Bromo-3-chloropropane → 3-Chloropropyl 1-phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-yl Ether

https://huagongshe.com/reaction/585459

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-olHCID 12148626—
SolventDimethylformamideHCID 6228—
Product3-Chloropropyl 1-phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-yl EtherHCID 1214863844.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 1-phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-ol (0.82 g, 2.7 mmol) in dry DMF (12 mL) is added 1-bromo-3chloropropane (1.28 g, 8.1 mmol) and potassium carbonate (1.12 g, 8.1 mmol). The mixture is heated at 80° C. for 6 h. The mixture is then stirred at room temperature for 18 h followed by another 6 h at 80° C. The mixture is partitioned between water and CH2Cl2. The organic layer is washed 3 times with water (100 mL). The organic layer is then dried over anhydrous sodium sulfate and concentrated. Column chromatography (60 mL silica) using hexanes/CH2Cl2 (1:1) as eluent gave an oil which is rechromatographed (60 mL silica) using hexanes/CH2C]2 (60/40) as eluent gave 0.454 g (44%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06932961B1
Source datasetuspto-grants-2005_08
ORD IDord-4a2466afeb6e45728fc780fa4200f347
Source noteuspto-grants-2005_08