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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411856Generated: November 1, 2026

Chlorotrimethylsilane → HCID 22323650, compound

https://huagongshe.com/reaction/411856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriphenylmethanesulfenyl ChlorideHCID 342378—
Reactant3-((2-Hydroxyethyl)amino)propanolHCID 3015059—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 22323650HCID 22323650—

Reaction Steps

N-(2-hydroxyethyl)-3-amino-1-propanol (5.0 g, 41.9 mmol) is coevaporated several times with pyridine (20 mL) and then dissolved in pyridine (100 mL). The reaction flask is flushed with Argon and trimethylsilylchloride (2.47 g, 209.5 mmol) is added dropwise. The reaction mixture is stirred for 1 hour. Triphenyl methanesulfenyl chloride (14.32 g, 46.09 mmol) is dissolved in CH2Cl2 and added via dropping funnel to the cooled reaction mixture. The reaction mixture is warmed to room temperature and stirred for 18 hours. The reaction mixture is concentrated in vacuo and the resultant residue is partitioned between H2O and EtOAc (100 ml, 1:1). The H2O layer is separated and extracted with EtOAc (3×50 ml). The EtOAc extracts are pooled, dried (MgSO4) and filtered. The filtrate is concentrated in vacuo and the residue is purified by silica gel flash column chromatography with EtOAc/hexanes as the eluent. The appropriate fractions are pooled and concentrated in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559303B1
Source datasetuspto-grants-2003_05
ORD IDord-990aa3d233b2451b872432b029293309
Source noteuspto-grants-2003_05