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HRID 1165445作成日:2026年10月27日

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

https://huagongshe.com/reaction/1165445

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Hydrochloric AcidHCID 313—
反応物Methane, dichloromethoxy-HCID 21004—
反応物4-Tert-butyl-3-methoxyphenolHCID 12252976—
触媒Titanium TetrachlorideHCID 24193—
溶媒DichloromethaneHCID 6344—
生成物2-Hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehydeHCID 1986182787%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04910202
出典データセットuspto-grants-1990_03
ORD IDord-8fd7d4478c3e4267980fcf98f96b7636
出典メモuspto-grants-1990_03