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

Water → HCID 14155946, 화합물

HRID 1253017
노트
인쇄 미리보기

반응식

HRID 1253017 반응식
[CH2:1]([O:3][C:4](=[O:15])[CH2:5][C:6]1[C:11]([C:12]([OH:14])=[O:13])=[CH:10][CH:9]=[CH:8][N:7]=1)[CH3:2].C(=O)(O)[O-].[Na+].[CH2:21](I)[CH3:22].O>CN(C)C=O>[CH2:1]([O:3][C:4](=[O:15])[CH2:5][C:6]1[C:11]([C:12]([O:14][CH2:21][CH3:22])=[O:13])=[CH:10][CH:9]=[CH:8][N:7]=1)[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6340IodoethaneHCID 516892Sodium BicarbonateHCID 27637332-(2-Ethoxy-2-oxoethyl)pyridine-3-carboxylic acid

생성물 1

HCID 14155946HCID 14155946, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
50 °C

실험 절차

To a mixture of 54 g (0.26 mole) of 3-carboxy-2-pyridineacetic acid ethyl ester* and 24.4 g (0.29 mole) of sodium bicarbonate in 300 ml of dimethylformamide was added 60.8 g (0.39 mole) of ethyliodide. The mixture was stirred at 50° C. for 24 hr; cooled to 25° C. and treated with 300 ml of water. The aqueous solution was extracted 3 times with isopropyl ether. The isopropyl ether solution was extracted with dilute hydrochloric acid. The acid layer was made basic with sodium hydroxide and extracted with isopropyl ether. The ether layer was dried over anhydrous sodium sulfate, concentrated and the residue was distilled to give 47 g (76%), b.p. 128°-130° C./0.5 mm.

후처리

  1. temperaturecooled to 25° C.
  2. extractionThe aqueous solution was extracted 3 times with isopropyl ether
  3. extractionThe isopropyl ether solution was extracted with dilute hydrochloric acid
  4. extractionextracted with isopropyl ether
  5. dry with materialThe ether layer was dried over anhydrous sodium sulfate
  6. concentrationconcentrated
  7. distillationthe residue was distilled
  8. customto give 47 g (76%), b.p. 128°-130° C./0.5 mm

출처 및 근거

ORD 기록
ord-b0ddac46811b46028653a9d8fd972d53
출처 데이터셋
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04746657

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트