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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1883941생성일: 2026년 10월 27일

Pyridine → Triethylammonium 2-[2-(4,4'-dimethoxytrityloxy)ethoxy] acetate

https://huagongshe.com/reaction/1883941

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DioxanoneHCID 18233—
반응물(2-Hydroxyethoxy)acetic acidHCID 25935—
반응물1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
생성물Triethylammonium 2-[2-(4,4'-dimethoxytrityloxy)ethoxy] acetateHCID 69912848—

반응 단계

A solution of 2-(2-hydroxyethoxy)acetic acid prepared as desctibed in (Snapp, Thomas C., Jr.; Blood, Alden E. Ether diester derivatives of p-dioxanone. U.S. (1975), 4 pp. U.S. Pat. No. 3,929,847) (7.45 g, 22 mmol) in pyridine (20 mL) is treated with 4,4′-dimethoxytrityl chloride (10.16 g, 30 mmol) overnight at room temperature and concentrated to an oil in vacuo. The residue is dissolved in a mixture of MeOH and CH2Cl2 (95:5, v/v; 200 mL) and washed with 2 M aqueous triethylammonium acetate (5×20 mL). The organic solution is evaporated, re-dissolved in CH2Cl2, dried over Na2SO4, and evaporated to give crude triethylammonium 2-[2-(4,4′-dimethoxytrityloxy) ethoxy] acetate in quantitative yield (10.47 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06762281B2
출처 데이터셋uspto-grants-2004_07
ORD IDord-d3a288449b8d4fcfb681b3ebd14fc522
출처 메모uspto-grants-2004_07