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Dimethylformamide → 2-Sulfo-2-(1-pyrryl)acetyl chloride

HRID 26319
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인쇄 미리보기

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HRID 26319 반응식
[S:1]([CH:5]([N:9]1[CH:13]=[CH:12][CH:11]=[CH:10]1)[C:6](O)=[O:7])([OH:4])(=[O:3])=[O:2].S(Cl)([Cl:16])=O.CN(C)C=O.CCCCCC>CCOCC>[S:1]([CH:5]([N:9]1[CH:13]=[CH:12][CH:11]=[CH:10]1)[C:6]([Cl:16])=[O:7])([OH:4])(=[O:3])=[O:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 8058HexaneHCID 24386Thionyl ChlorideHCID 867364652-Sulfo-2-(1-pyrryl)acetic acid

생성물 1

HCID 867364672-Sulfo-2-(1-pyrryl)acetyl chloride

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

반응 조건

온도
40 °C

실험 절차

2-Sulfo-2-(1-pyrryl)acetic acid is treated with thionyl chloride in ether at room temperature according to the general procedure in J. Med. Chem., 15, 1105 (1972) until the evolution of gas stops. Dimethylformamide is added, the solution is warmed to about 40° C. for 1 hour. Then ether is added, followed by hexane and the solution cooled to about -25° C. 2-Sulfo-2-(1-pyrryl)acetyl chloride is isolated from the solvent by decantation.

후처리

  1. temperaturethe solution cooled to about -25° C

출처 및 근거

ORD 기록
ord-e1561fb8a76442beaa3c4d1d9f935f62
출처 데이터셋
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04148998

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