HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531449Generated: October 29, 2026
Chlorotrimethylsilane → HCID 22323650, compound
https://huagongshe.com/reaction/1531449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triphenylmethanesulfenyl Chloride | HCID 342378 | — |
| Reactant | 3-((2-Hydroxyethyl)amino)propanol | HCID 3015059 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22323650 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06197965B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-b8c4901269bb44d09895c477633b6605 |
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| Source note | uspto-grants-2001_03 |
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