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HRID 1180040作成日:2026年10月27日

Trifluoroacetic acid → 4-[4-(2-Pyrrolidin-1-yl-ethoxy)-benzyl]-phenol

https://huagongshe.com/reaction/1180040

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物TriethylsilaneHCID 12052—
反応物p-((Trimethylsilyl)oxy)benzaldehydeHCID 70536—
反応物N-(2-(p-bromophenoxy)ethyl)pyrrolidineHCID 70657—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物4-[4-(2-Pyrrolidin-1-yl-ethoxy)-benzyl]-phenolHCID 2204796594.3%

反応手順

To a stirred solution of 1-[2-(4-bromo-phenoxy)-ethyl]-pyrrolidine (2.89 g, 10.7 mmol) in THF (30 mL) was added dropwise 1.6 M solution in hexanes n-BuLi (7 mL, 10.2 mmol) over a 5-min period at −78° C. The mixture was stirred at −78° C. for 15 min before 4-trimethylsilyloxybenzaldehyde (2.08 g, 10.7 mmol) was added. The mixture was allowed to warm to rt during 20 min and quenched with water. Extraction with CH2Cl2, drying (MgSO4), filtration and evaporation provided the crude diarylmethanol which was dissolved in CH2Cl2 (30 mL) and stirred with triethylsilane (4 mL) and TFA (5 mL) for 16 h at rt. Evaporation gave 3.0 g (84%) 4-[4-(2-pyrrolidin-1-yl-ethoxy)-benzyl]-phenol. This was carbamoylated using general procedure 1 (CH2Cl2 was used as solvent) to give the title product after purification by preparative HPLC (Gilson) (35%, oil).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07279470B2
出典データセットuspto-grants-2007_10
ORD IDord-47bbc5c9258c42a59a954da5675c2c30
出典メモuspto-grants-2007_10