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HRID 1165445Erstellt: 26. Oktober 2026
Benzaldehyde → 2-Hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehyde
https://huagongshe.com/reaction/1165445
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Methane, dichloromethoxy- | HCID 21004 | — |
| Edukt | 4-Tert-butyl-3-methoxyphenol | HCID 12252976 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehyde | HCID 19861827 | 87% |
Reaktionsschritte
The benzaldehyde used in Example 6 was prepared as follows: (1) To a stirred solution of 2.91 g (16.14 mmol) of 3-methoxy-4-(1,1-dimethylethyl)phenol (see C. J. R. Adderley and F. R. Hewgill, J. Chem. Soc., (C), 1438, (1968) as an example of how to obtain this material) in 65 ml of methylene chloride and cooled in an ice-water bath was added 6.12 g (3.54 ml, 32.30 mmol) of titanium (IV) chloride followed by 3.06 g (2.41 ml, 26.64 mmol) of 1,1-dichlorodimethyl ether. The reaction mixture was stirred for 10 minutes and then poured into 16 ml of lN hydrochloric acid. The organic phase was separated, dried and evaporated. The residue was chromatographed on silica gel (146 g) using 1.5:98.5 (v/v) ether,hexane as eluent. There was obtained 2.92 g (14.01 mmol, 87%) of 2-hydroxy-4-methoxy-5-(1,1-dimethylethyl)benzaldehyde as a white solid after crystallization from pentane; mp 75°-78° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04910202 |
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| Quelldatensatz | uspto-grants-1990_03 |
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| ORD ID | ord-8fd7d4478c3e4267980fcf98f96b7636 |
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| Quellennotiz | uspto-grants-1990_03 |
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