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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130348생성일: 2026년 10월 24일

Ammonium Chloride → (3-(1,3-Dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-ol

https://huagongshe.com/ko/reaction/130348

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물3-(Trifluoromethyl)benzaldehydeHCID 67990—
반응물2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물(3-(1,3-Dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-olHCID 69255414—

반응 단계

A 1.0 mL aliquot of 2-(3-bromophenyl)-1,3-dioxolane is added into magnesium (610 mg; 25 mmol) and THF (5 mL) under Argon. After the reaction is started, the residue of 2-(3-bromophenyl)-1,3-dioxolane (total: 5.73 g; 25 mmol) in THF (20 mL) is added dropwise into the reaction mixture. The resulting solution is stirred at room temp for six hours, and then at 50-60° C. for 20 hours. After the mixture is cooled, a solution of 3-(trifluoromethyl)-benzaldehyde (4.35 g; 25 mmol) in THF (20 mL) is added dropwise and the reaction is stirred at room temp for 24 hours. A saturated solution of NH4Cl (50 mL) is added and stirred for 30 minutes. The organic layer is separated and the aqueous layer is extracted with ethyl acetate (2×100 mL). The organic layers are combined and dried over anhydrous Na2SO4. The solvent is removed and the residue is purified by column chromatography on silica gel. Eluting with ethyl acetate/hexanes (20:80) provide a colorless oil (3.23 g; 40%) as (3-(1,3-dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-ol: MS 307.0 (M−17).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381736B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-d5bd1ef900304afea4d5fb5210705be1
출처 메모uspto-grants-2008_06