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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247376Generated: October 26, 2026

Sodium hydride → HCID 14031259, compound

https://huagongshe.com/reaction/247376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantPhenoxazineHCID 67278—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14031259HCID 14031259—

Reaction Steps

5 Grams of phenoxazine was dissolved in 100 ml of dry tetrahydrofuran, then 1.63 g of 50% sodium hydride in mineral oil was added and the mixture refluxed for 30 minutes. Then 6.19 g of t-butyldimethylsilyl chloride in dimethylformamide (2 ml) and tetrahydrofuran (8 ml) was added and reflux was continued for five more minutes. The reaction was quenched by the addition of water, the organic layer was separated and dried over sodium sulfate. Then the solvent was removed under reduced pressure and the residue purified by column chromatography (silica as solid phase, hexane:ethylacetate (95:5) as mobile phase). N-t-butyldimethylsilylphenoxane had a melting point of 57° C. after crystallization from pentane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04707473
Source datasetuspto-grants-1987_11
ORD IDord-ff27321f287a4e1ead576b4f6dfe71a7
Source noteuspto-grants-1987_11