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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1165445생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1165445

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Hydrochloric AcidHCID 313—
반응물Methane, dichloromethoxy-HCID 21004—
반응물4-Tert-butyl-3-methoxyphenolHCID 12252976—
촉매Titanium TetrachlorideHCID 24193—
용매DichloromethaneHCID 6344—
생성물2-Hydroxy 4-methoxy-5-(1,1-dimethylethyl)benzaldehydeHCID 1986182787%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04910202
출처 데이터셋uspto-grants-1990_03
ORD IDord-8fd7d4478c3e4267980fcf98f96b7636
출처 메모uspto-grants-1990_03