HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247378Generated: October 29, 2026
Sodium borohydride → HCID 21276372, compound
https://huagongshe.com/reaction/247378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14031260 | HCID 14031260 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21276372 | HCID 21276372 | — |
Reaction Steps
A mixture of 3.9 g (12.3 mmoles) of 4-formyl-N-(α-phenylethyl)phenoxazine, 250 ml of ethanol and 0.594 g (18.5 mmoles) of sodium borohydride was heated at 40° C. under stirring during 15 minutes. The solvent was then removed under reduced pressure and the residue diluted with water and extracted with ethyl acetate (2×100 ml). The combined extracts were dried and the solvent removed under reduced pressure. The oily residue (3.5 g) was percolated through a short column of silica gel using ether as the solvent, to yield 4-hydroxymethyl-N-(α-phenylethyl)phenoxazine, as an oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04707473 |
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| Source dataset | uspto-grants-1987_11 |
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| ORD ID | ord-d98aa8fbc22542888cc106808c0a03d3 |
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| Source note | uspto-grants-1987_11 |
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