HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48087Erstellt: 23. Oktober 2026
Hydrochloric Acid → 3-((Tert-butyldimethylsilyl)oxy)propanal
https://huagongshe.com/de/reaction/48087
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 3-[(Tert-butyldimethylsilyl)oxy]propan-1-ol | HCID 4077791 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-((Tert-butyldimethylsilyl)oxy)propanal | HCID 3662392 | — |
Reaktionsschritte
DMSO (24 mmol) is added to oxalyl chloride (11 mmol) in 40 mL of CH2Cl2 cooled to −78° C. After 15 minutes, alcohol 46 (10 mmol) is added. After an additional 15 minutes, triethylamine (50 mmol) is added. The mixture is allowed to warm to 0° C. and then poured into 0.1 M HCl (100 mL). The phases are separated, and the aqueous phase is extracted with ethyl acetate (2×100 mL). The organic phases are washed with water (100 mL), dried over anhydrous MgSO4, and concentrated in vacuo. The mixture is purified by flash chromatography to give the product as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06702705B1 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-5c15f2fb99da45d49beebf1bfbf5498f |
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| Quellennotiz | uspto-grants-2004_03 |
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