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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761714Generated: November 3, 2026

Phenylethanolamine → HCID 14624895, compound

https://huagongshe.com/reaction/1761714

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 dimethylsiloxy1-ethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04827006
Source datasetuspto-grants-1989_05
ORD IDord-a1e4817cf4c04027a9aa050268ceb0c5
Source noteuspto-grants-1989_05