Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637678Generated: November 2, 2026

1-Bromo-3-chloropropane → 10-(3-Chloropropyl)-10H-phenoxazine

https://huagongshe.com/reaction/1637678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantPhenoxazineHCID 67278—
SolventDimethylformamideHCID 6228—
Product10-(3-Chloropropyl)-10H-phenoxazineHCID 10083926—

Reaction Steps

To a solution of phenoxazine (3.7 g, 0.02 mol) in dry dimethylformamide (100 ml) kept under an atmosphere of nitrogen, sodium hydride (1.2 g, 0.03 mol 60% dispersion in oil) was carefully added. The reaction mixture was left stirring for 15 minutes. 1-Bromo-3-chloro-propane (8.0 g, 0.05 mol) was added and the mixture was left stirring overnight. Ammonium chloride (2.0 g, 0.04 mol) was added, and after continued stirring for 30 minutes, the solution was poured onto water (300 ml). The mixture was extracted with dichloromethane (2×200 ml). The combined organic extracts were dried (MgSO4), filtered and the solvent evaporated in vacuo. 10-(3-Chloropropyl)-10H-phenoxazine was obtained in quantitative yield as an oil and used without further purification. Rf : 0.68 (SiO2 ; n-heptane/ethyl acetate (1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06043239
Source datasetuspto-grants-2000_03
ORD IDord-ec657ba361434106a89e9dce783b2eae
Source noteuspto-grants-2000_03