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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 257355생성일: 2026년 10월 24일

Formaldehyde → 4-Chloro-2-hydroxybenzaldehyde

https://huagongshe.com/ko/reaction/257355

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물3-ChlorophenolHCID 7933—
반응물TetrahydrofuranHCID 8028—
반응물HexamethylphosphoramideHCID 12679—
반응물HCID 178418443HCID 178418443—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물4-Chloro-2-hydroxybenzaldehydeHCID 52010173.5%

반응 조건

온도80 °C

반응 단계

A 2M solution of ethylmagnesium bromide in tetrahydrofuran (50 ml, 0.10 mole) was placed in a flask, and a solution of 12.85 g (0.10 mole) of 3-chlorophenol in 50 mL of diethyl ether was added slowly with stirring. The addition required two hours, after which the solvents were removed by evaporation under reduced pressure. Toluene (200 ml), 7.50 g (0.25 mole) of paraformaldehyde, and 17.92 g (0.10 mole) of hexamethylphosphoramide were added to the residue, and this mixture was heated at 80° C. for approximately 16 hours. The solvent was evaporated under reduced pressure, leaving a residue. This residue was washed successively with 50 mL of hydrochloric acid and 300 mL of water. Vacuum distillation of the washed residue yielded 11.50 g of 4-chlorosalicylaldehyde, b.p. 112° C. at 9 mm of Hg. This reaction was repeated several times.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05262390
출처 데이터셋uspto-grants-1993_11
ORD IDord-e8df0bebc4294be48db9951d1906c2d9
출처 메모uspto-grants-1993_11