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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247378Generated: October 29, 2026

Sodium borohydride → HCID 21276372, compound

https://huagongshe.com/reaction/247378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14031260HCID 14031260—
SolventEthanolHCID 702—
ProductHCID 21276372HCID 21276372—

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04707473
Source datasetuspto-grants-1987_11
ORD IDord-d98aa8fbc22542888cc106808c0a03d3
Source noteuspto-grants-1987_11