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HRID 130348作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物3-(Trifluoromethyl)benzaldehydeHCID 67990—
反応物2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物(3-(1,3-Dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-olHCID 69255414—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381736B2
出典データセットuspto-grants-2008_06
ORD IDord-d5bd1ef900304afea4d5fb5210705be1
出典メモuspto-grants-2008_06