돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1180040생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1180040

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylsilaneHCID 12052—
반응물p-((Trimethylsilyl)oxy)benzaldehydeHCID 70536—
반응물N-(2-(p-bromophenoxy)ethyl)pyrrolidineHCID 70657—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물4-[4-(2-Pyrrolidin-1-yl-ethoxy)-benzyl]-phenolHCID 2204796594.3%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07279470B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-47bbc5c9258c42a59a954da5675c2c30
출처 메모uspto-grants-2007_10