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Hydrochloric Acid → 3-Chloro-4-(pyrrolidin-1-ylsulfonyl)benzonitrile

HRID 2053923
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HRID 2053923 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]#[N:9])[CH:5]=[CH:4][C:3]=1[S:10](Cl)(=[O:12])=[O:11].[NH:14]1[CH2:18][CH2:17][CH2:16][CH2:15]1.Cl>N1C=CC=CC=1>[Cl:1][C:2]1[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=1[S:10]([N:14]1[CH2:18][CH2:17][CH2:16][CH2:15]1)(=[O:12])=[O:11])[C:8]#[N:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 31268PyrrolidineHCID 27357222-Chloro-4-cyanobenzene-1-sulfonyl chloride

생성물 1

HCID 693125003-Chloro-4-(pyrrolidin-1-ylsulfonyl)benzonitrile

시약·촉매·용매 1

HCID 1049Pyridine용매

반응 조건

온도
80 °C

실험 절차

900 mg (4 mmol) of 2-chloro-4-cyanobenzenesulfonic acid chloride is dissolved in 3 mL of pyridine and, after the addition of 0.5 mL (5.8 mmol) of pyrrolidine, stirred for one hour at 80° C. Then the mixture is cooled, mixed with ice, and adjusted to pH 5-6 with 1 molar hydrochloric acid. The precipitate formed is suction filtered, washed with water and dried. Yield: 1.1 g (100% of theory); Rf value: 0.20 (silica gel; petroleum ether/ethyl acetate=4:1).

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후처리

  1. temperatureThen the mixture is cooled
  2. additionmixed with ice
  3. customThe precipitate formed
  4. filtrationfiltered
  5. washwashed with water
  6. customdried

출처 및 근거

ORD 기록
ord-3b00fd508f5847b9828189c119564c17
출처 데이터셋
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07326791B2

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