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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4693생성일: 2026년 10월 24일

Hydrochloric Acid → 5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedimethanol

https://huagongshe.com/ko/reaction/4693

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물PhenolHCID 996—
반응물4-tert-ButylphenolHCID 7393—
반응물Sodium HydroxideHCID 14798—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물5-(1,1-Dimethylethyl)-2-hydroxy-1,3-benzenedimethanolHCID 150981—

반응 단계

50 g sodium hydroxide were dissolved in approximately 1.2 liters of water, and 150 g of 4-tert-butylphenol were added to this solution. The mixture was stirred and gently heated until the phenol dissolved. The solution was then cooled to ambient temperature. Aqueous formaldehyde (175 ml, 37 percent) was added, and the solution was stirred for four to six days at ambient temperature. Concentrated hydrochloric acid (110 ml) was added, upon which a two-phase system forms. A yellow, oily organic phase was isolated and washed with three 500 ml portions of water. Chloroform (700 ml) and 500 ml of water were added to this organic oil and the mixture was stirred. The organic phase was isolated and dried over 100 g of anhydrous magnesium sulphate. Evaporation and cooling of the chloroform solution yielded a mixture of white crystals and oil. The addition of 50-100 ml of chloroform and filtration yielded a white crystalline product, 4-tert-butyl-2,6-di(hydroxymethyl)phenol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727123
출처 데이터셋uspto-grants-1988_02
ORD IDord-0970fc1f0ddc4dc68f97748679c31c19
출처 메모uspto-grants-1988_02