돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 510324생성일: 2026년 10월 23일

Methyl bromoacetate → 1,1-Bis-(4-hydroxyphenyl)-1-(4-methoxycarbonylmethoxyphenyl)ethane

https://huagongshe.com/ko/reaction/510324

반응식

참여 물질

역할이름HCID투입량
반응물Methyl bromoacetateHCID 60984—
반응물1,1,1-Tris(4-hydroxyphenyl)ethaneHCID 93118—
촉매Potassium IodideHCID 4875—
용매AcetoneHCID 180—
생성물1,1-Bis-(4-hydroxyphenyl)-1-(4-methoxycarbonylmethoxyphenyl)ethaneHCID 1171781385.1%

반응 단계

Methyl bromoacetate (0.48 mL, 5 mmol) was added dropwise to an acetone solution (10 mL) including 1,1,1-tris(4-hydroxyphenyl)ethane (1.53 g, 5 mmol) potassium carbonate (0.79 g, 5 mmol) and potassium iodide (16 mg, 0.1 mmol). The addition was done at room temperature under argon. The mixture was refluxed for 24 h, and then it was cooled to room temperature and extracted with ethyl acetate. The combined organic layer was washed with 3% aqueous NaHCO3, a saturated brine solution, dried (Na2SO4) and then evaporated to dryness to give 1.61 g (85% yield) of the desired compound as a colorless semisolid. 1H-NMR (300 MHz, d6-DMSO): 1.96 [s, 3H, —CH3], 3.67 [s, 3H, —OCH3], 4.71 [s, 4H, —OCH2—], 6.57-6.64 [m, 4H, Ar—H], 6.72-6.81 [m, 6H, Ar—H], 6.85-6.92 [m, 2H, Ar—H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096607B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-bc0e8b82de0849fa90dc3c84ba4aec06
출처 메모uspto-grants-2015_08