홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Diethyl Oxalate → 2,4-Dioxo-4-thiazol-2-yl-butyric acid ethyl ester

HRID 129835
노트
인쇄 미리보기

반응식

HRID 129835 반응식
[C:1]([O:8][CH2:9][CH3:10])(=[O:7])[C:2]([O:4]CC)=O.[C:11]([C:14]1[S:15][CH:16]=[CH:17][N:18]=1)(=[O:13])[CH3:12]>[O-]CC.[Na+]>[CH2:9]([O:8][C:1](=[O:7])[C:2](=[O:4])[CH2:12][C:11](=[O:13])[C:14]1[S:15][CH:16]=[CH:17][N:18]=1)[CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7268Diethyl OxalateHCID 5201082-Acetylthiazole

생성물 1

HCID 537614132,4-Dioxo-4-thiazol-2-yl-butyric acid ethyl ester수율 72.2%

시약·촉매·용매 1

HCID 2723922Sodium ethoxide용매

실험 절차

To a sodium ethoxide solution (prepared from 150 ml of ethanol and 4.2 g of sodium) at 0° C., a mixture of diethyl oxalate (22.98 g) and acetylthiazole (20.07 g) was added dropwise. The resulting mixture was stirred at room temperature for 2 hours and concentrated. The residue was treated with 100 ml of water and neutralized with 6N HCl. Filtration afforded 25.8 g of 2,4-diketo-4-(thiazol-2-yl)butyric acid ethyl ester as brown solids. NMR: 1.46 (t, 3H), 4.49 (q, 2H), 7.27 (s, 1H), 7.65, 8.04 (2d, 2H, thiazolyl H's).

후처리

  1. additionwas added dropwise
  2. concentrationconcentrated
  3. additionThe residue was treated with 100 ml of water and neutralized with 6N HCl
  4. filtrationFiltration

출처 및 근거

ORD 기록
ord-07e4f8c57880493e91f3b448105bb0cd
출처 데이터셋
uspto-grants-1995_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05470862

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트