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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034073Generated: October 25, 2026

Phenoxazine → Methyl 3-(phenoxazin-10-ylmethyl)benzoate

https://huagongshe.com/reaction/1034073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenoxazineHCID 67278—
ReactantMethyl 3-(chloromethyl)benzoateHCID 3248988—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(phenoxazin-10-ylmethyl)benzoateHCID 1902478928.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of phenoxazine (2.20 g) in tetrahydrofuran (30 ml) was added potassium tert-butoxide (2.69 g) at 0° C. The mixture was stirred at 0° C. for 10 minutes, and then a solution of methyl 3-(chloromethyl)benzoate (2.44 g) in tetrahydrofuran (20 ml) was added. The mixture was stirred at 25° C. for 30 minutes, and then evaporated. The residue was partitioned between ethyl acetate and 0.1N hydrochloric acid. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was purified by chromatography on silica gel eluting with a mixture of hexane and ethyl acetate (40:1-20:1) and recrystallization from a mixture of hexane and ethyl acetate to give e methyl 3-(phenoxazin-10-ylmethyl)benzoate (1.12 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312829
Source datasetuspto-grants-1994_05
ORD IDord-2ca1e970ada74c3e9e9774259efa1816
Source noteuspto-grants-1994_05