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Water → Methyl 3-(2-cyanopyrrol-1-yl)benzoate

HRID 399863
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HRID 399863 반응식
ClS([N:5]=[C:6]=O)(=O)=O.[N:8]1([C:13]2[CH:14]=[C:15]([CH:20]=[CH:21][CH:22]=2)[C:16]([O:18][CH3:19])=[O:17])[CH:12]=[CH:11][CH:10]=[CH:9]1.CN(C)C=O.O>ClCCl>[C:6]([C:12]1[N:8]([C:13]2[CH:14]=[C:15]([CH:20]=[CH:21][CH:22]=2)[C:16]([O:18][CH3:19])=[O:17])[CH:9]=[CH:10][CH:11]=1)#[N:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6228DimethylformamideHCID 70918Chlorosulfonyl isocyanateHCID 3322314Methyl 3-(1H-pyrrol-1-yl)benzoate

생성물 1

HCID 18945318Methyl 3-(2-cyanopyrrol-1-yl)benzoate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Chlorosulfonyl isocyanate (18.2 ml) was dropwise added to a solution of methyl 3-(pyrrol-1-yl)benzoate (35.0 g) in dichloromethane (350 ml) at -10°~20° C. and the mixture was stirred for 1 hour at the same temperature. To the mixture was dropwise added N,N-dimethylformamide (105 ml) at the same temperature and the mixture was stirred for 1 hour at 0°-5° C. The reaction mixture was poured into water. The separated organic layer was washed with saturated aqueous sodium bicarbonate solution and water. The organic solution was dried over magnesium sulfate and evaporated in vacuo to give methyl 3-(2-cyanopyrrol-1-yl)benzoate (30.67 g).

후처리

  1. stirringthe mixture was stirred for 1 hour at 0°-5° C
  2. washThe separated organic layer was washed with saturated aqueous sodium bicarbonate solution and water
  3. dry with materialThe organic solution was dried over magnesium sulfate
  4. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-9a1d0727ce7e4f48b6f76e523f48377d
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05824691

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