HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 576338Erstellt: 24. Oktober 2026
Phenetole → (5-Bromo-2-chloro-3-methoxyphenyl)(4-ethoxyphenyl)methanone
https://huagongshe.com/de/reaction/576338
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenetole | HCID 7674 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Edukt | 5-Bromo-2-chloro-3-methoxybenzoic acid | HCID 71076961 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (5-Bromo-2-chloro-3-methoxyphenyl)(4-ethoxyphenyl)methanone | HCID 71076739 | — |
Reaktionsschritte
To a solution of acid 56 (4.9 g, 18.57 mmol) in CH2Cl2 (62 mL) were added oxalyl chloride (2.1 mL, 24.14 mmol) and catalytic amounts of DMF at room temperature. The mixture was stirred at room temperature for 3 hours. The mixture was evaporated in vacuo and dried under high vacuum. The crude acid chloride was dissolved with CH2Cl2 (93 mL) and cooled to 0° C. To the mixture was added phenetole (2.4 mL, 18.57 mmol) at 0° C. and stirred at 0° C. for 5 min. To the reaction mixture was added AlCl3 (2.7 g, 20.43 mmol) portionwise at 0° C. The mixture was stirred at 0° C. for 30 min, warmed up to room temperature and stirred at room temperature for 15 hours. The mixture was poured into ice-water and extracted with CH2Cl2 (100 mL×2). The combined organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The crude product 73 was dried under high vacuum and used without further purification (7.0 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09034921B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-b2b7fc3b24c249028b4d40061bc7c671 |
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| Quellennotiz | uspto-grants-2015_05 |
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