HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1977718Erstellt: 26. Oktober 2026
Hydrochloric Acid → Benzenemethanol, 4-chloro-alpha-(1-methylethyl)-
https://huagongshe.com/reaction/1977718
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Isobutyraldehyde | HCID 6561 | — |
| Edukt | HCID 178478191 | HCID 178478191 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Benzenemethanol, 4-chloro-alpha-(1-methylethyl)- | HCID 202426 | — |
Reaktionsschritte
A 1 M solution of p-chlorophenylmagnesium bromide in diethyl ether (100 mL) is added to a solution of isobutyraldehyde (9.08 mL, 0.1 mol) in diethyl ether at −5° C. After the addition is complete, the reaction mixture is stirred overnight at room temperature, diluted with an ice-water mixture, and acidified with 10% hydrochloric acid. The phases are separated and the aqueous phase is extracted with diethyl ether. The organic phase and extracts are combined, washed sequentially with saturated sodium hydrogen carbonate solution, water and brine, dried over anhydrous sodium sulfate, and concentrated in vacuo to obtain an oil. Column chromatography of the oil using silica gel and a 33% methylene chloride in hexanes solution gives the title product as a colorless oil (14 g) which is identified by NMR spectral analyses.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06235754B1 |
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| Quelldatensatz | uspto-grants-2001_05 |
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| ORD ID | ord-7e729b22eb1046158e8f392dec2a5cf0 |
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| Quellennotiz | uspto-grants-2001_05 |
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