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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenoxazine | HCID 67278 | — |
| Reactant | Methyl 3-(chloromethyl)benzoate | HCID 3248988 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-(phenoxazin-10-ylmethyl)benzoate | HCID 19024789 | 28.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05312829 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-2ca1e970ada74c3e9e9774259efa1816 |
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| Source note | uspto-grants-1994_05 |
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