HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219779Generated: October 26, 2026
Aluminium lithium hydride → 10H-Phenoxazine-10-ethanol
https://huagongshe.com/reaction/2219779
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl-2-(10H-phenoxazin-10-yl)acetate | HCID 53780817 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 10H-Phenoxazine-10-ethanol | HCID 10176924 | 99% |
Reaction Steps
A solution of ethyl-2-(10H-phenoxazin-10-yl)acetate (5.5 g, 20.44 mmol) in dry tetrahydrofuran (20 ml) was added dropwise to a suspension of lithium aluminum hydride (1.16 g, 30.52 mmol) in dry tetrahydrofurane (20 ml) at 0° C. The reaction mixture was warmed to room temperature and stirred for additional 1 h. The excess lithium aluminum hydride was quenched with a solution of saturated sodium sulfate at 0° C. The reaction mixture was filtered and the residue was washed with hot ethyl acetate (2×75 ml). The combined organic layers were dried (Na2SO4), filtered and the solvent was evaporated under reduced pressure to afford the title compound (4.6 g, 99%) as a colourless solid. The compound is used in the next step without further purification. mp: 113-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414128B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-daf83ead28c445b18b28d3c3facb92c8 |
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| Source note | uspto-grants-2008_08 |
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