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HRID 1165445Erstellt: 26. Oktober 2026

Benzaldehyde → 2-Hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehyde

https://huagongshe.com/reaction/1165445

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktHydrochloric AcidHCID 313—
EduktMethane, dichloromethoxy-HCID 21004—
Edukt4-Tert-butyl-3-methoxyphenolHCID 12252976—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehydeHCID 1986182787%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04910202
Quelldatensatzuspto-grants-1990_03
ORD IDord-8fd7d4478c3e4267980fcf98f96b7636
Quellennotizuspto-grants-1990_03