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Thionyl Chloride → HCID 53808777, 화합물

HRID 1579384
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반응식

HRID 1579384 반응식
S(Cl)([Cl:3])=O.[O:5]=[C:6]1[C:15]2[C:10](=[N:11][CH:12]=[CH:13][CH:14]=2)[O:9][C:8]2[CH:16]=[CH:17][C:18]([C:20]([O-:22])=O)=[CH:19][C:7]1=2.[Na+]>C(Cl)(Cl)(Cl)Cl>[O:5]=[C:6]1[C:15]2[C:10](=[N:11][CH:12]=[CH:13][CH:14]=2)[O:9][C:8]2[CH:16]=[CH:17][C:18]([C:20]([Cl:3])=[O:22])=[CH:19][C:7]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 23687371HCID 23687371, 화합물

생성물 1

HCID 53808777HCID 53808777, 화합물

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

2.5 g of thionyl chloride is added to a suspension of 4.5 g of sodium 5-oxo-5H-[1]benzopyrano[2,3-b]pyridine-7-carboxylate in 35 ml of carbon tetrachloride with stirring, and the mixture is stirred under reflux for 3 hours. After cooling, the crystals are filtered off, washed with cool water and then with acetone, and dried to give 5-oxo-5H-[1]benzopyrano[2,3-b]pyridine-7-carboxylic acid chloride melting at 234°-235°C.

후처리

  1. stirringthe mixture is stirred
  2. temperatureunder reflux for 3 hours
  3. temperatureAfter cooling
  4. filtrationthe crystals are filtered off
  5. washwashed with cool water
  6. dry with materialwith acetone, and dried

출처 및 근거

ORD 기록
ord-aa79734630ba4e82a7d9a0fe73244bac
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03931199

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