Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → Triethylammonium 2-[2-(4,4'-dimethoxytrityloxy)ethoxy] acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Dioxanone | HCID 18233 | — |
| 반응물 | (2-Hydroxyethoxy)acetic acid | HCID 25935 | — |
| 반응물 | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| 생성물 | Triethylammonium 2-[2-(4,4'-dimethoxytrityloxy)ethoxy] acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06762281B2 |
| 출처 데이터셋 | uspto-grants-2004_07 |
| ORD ID | ord-d3a288449b8d4fcfb681b3ebd14fc522 |
| 출처 메모 | uspto-grants-2004_07 |