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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788677Generated: November 1, 2026

Triethylamine → O-(tert-Butyldiphenylsilyl)hydroxylamine

https://huagongshe.com/reaction/1788677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventDimethylformamideHCID 6228—
ProductO-(tert-Butyldiphenylsilyl)hydroxylamineHCID 11737343—

Reaction Steps

Hydroxylamine hydrochloride (3.48 g) and triethylamine (7 ml) were stirred for 0.25 hours in DMF (50 ml) at 0° C. tert-Butyldiphenylsilyl chloride (13 ml) was added and the mixture was stirred for 1 hour. The mixture was partitioned between pentane (500 ml) and water (100 ml), the layers separated and the aqueous phase extracted with ethyl acetate (2×100 ml). The organic layers were combined, washed with brine (50 ml), dried over magnesium sulphate and the solvent was removed in vacuo. The crude product was triturated with pentane (20 ml) yielding the pure title compound as white solid (4.04 g), m.p.t. 85°-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684641
Source datasetuspto-grants-1987_08
ORD IDord-87387689be1e4fb4aa903dde6aeb2236
Source noteuspto-grants-1987_08