HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748792Generated: October 25, 2026
Imidazole → 2-[2-(t-Butyldiphenylsilyloxy)ethylthio]ethanol
https://huagongshe.com/reaction/748792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Thiodiglycol | HCID 5447 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2-(t-Butyldiphenylsilyloxy)ethylthio]ethanol | HCID 59750807 | 54.2% |
Reaction Steps
In dichloromethane (200 ml) were dissolved 2,2′-thiodiethanol (10.0 g, 81.8 mmol) and imidazole (4.70 g, 69.0 mmol), followed by the dropwise addition of t-butylchlorodiphenylsilane (15.0 ml, 57.7 mmol) at room temperature. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 14 hours. After concentration under reduced pressure, diethyl ether was added to the residue. Then, the insoluble matter was filtered off. The residue obtained by concentrating the filtrate under reduced pressure was subjected to flash silica gel chromatography, and the fraction obtained from the hexane:ethyl acetate=3:1 eluate was concentrated under reduced pressure, whereby the title compound (11.3 g, 31.3 mmol, 54%) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399775B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-b676ef213e204279a50daff62ebef92f |
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| Source note | uspto-grants-2008_07 |
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