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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085311Generated: November 1, 2026

Phenylethanolamine → HCID 14624895, compound

https://huagongshe.com/reaction/1085311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylethanolamineHCID 1000—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
SolventDichloromethaneHCID 6344—
ProductHCID 14624895HCID 14624895—

Reaction Steps

To a solution of 1-phenyl-2-aminoethanol (5.323 g, 38.80 mmole) in 50 mL dichloromethane was added tert-butyldimethylsilyl chloride (7.030 g, 46.63 mmole) followed, after 15 minutes by tetramethylguanidine (2.430 g, 21.09 mmole). The reaction mixture was stirred at room temperature for 15 minutes and quenched by addition of water (40 mL). Layers were separated. The aqueous phase was extracted with dichloromethane (40 mL). Combined organic phases were washed with brine (2×50 mL), dried over magnesium sulfate and concentrated in vacuo to give crude 2-phenyl-2-tert-butyl dimethylsiloxy-1-ethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008404
Source datasetuspto-grants-1991_04
ORD IDord-52852a77a8f64288b17b495e04d136f8
Source noteuspto-grants-1991_04