돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1528513생성일: 2026년 10월 24일

Trifluoroacetic acid → (Hydroxy-(3,4,5-trimethoxy-phenyl)-methyl]-phosphonic acid dimethyl ester

https://huagongshe.com/ko/reaction/1528513

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물3,4,5-TrimethoxybenzaldehydeHCID 6858—
반응물Dimethyl phosphate anionHCID 3753418—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
생성물(Hydroxy-(3,4,5-trimethoxy-phenyl)-methyl]-phosphonic acid dimethyl esterHCID 1410168788%

반응 조건

온도0 °C

반응 단계

A round-bottom flask equipped with thermometer, condenser and gas inlet was charged with methanol (150 mL) and sodium methoxide (1.074 g, 20 mmol) and cooled to 0° C. under nitrogen protection. To a stirred solution were added subsequently dimethyl phosphate (19.52 g, 0.177 mol) and 3,4,5-trimethoxybenzaldehyde (30 g, 0.153 mol). A resulted solution was heated at 50° C. for 1 hour, cooled down to r.t. and treated with trifluoroacetic acid (4.6 ml). The mixture was concentrated under reduced pressure, the residue dissolved in EtOAc (300 mL), washed once with 18% brine, then once with saturated brine, dried over sodium sulfate. The filtered solution was concentrated until precipitation started. To the resulted suspension 1:1 mixture of t-butylmethyl ether and heptane was added (50 mL). Solid was filtered out, washed with two portions (20 mL) of the same solvent mixture and vacuum-dried to give 41.2 g (88%) of 1, LC purity 99.4% (AUC), m.p. 103-104° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09090603B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-c3c7108e2a6a418b9451c418b4763fb0
출처 메모uspto-grants-2015_07