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3-(2-Nitroethenyl)thiophene → HCID 53948007, 화합물

HRID 487314
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HRID 487314 반응식
[N+:1]([CH:4]=[CH:5][C:6]1[CH:10]=[CH:9][S:8][CH:7]=1)([O-:3])=[O:2].[CH3:11][Al](C)C>CCCCCC>[N+:1]([CH2:4][CH:5]([C:6]1[CH:10]=[CH:9][S:8][CH:7]=1)[CH3:11])([O-:3])=[O:2]
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참가 물질

4

반응물 2

HCID 27324183-(2-Nitroethenyl)thiopheneHCID 16682925Trimethylaluminum

생성물 1

HCID 53948007HCID 53948007, 화합물수율 80%

시약·촉매·용매 1

HCID 8058Hexane용매2회

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온도
5 °C

실험 절차

When R2 was H, the 3-(2-nitroethenyl)thiophene (1 eq) was suspended in hexane, cooled to 5° C. in an ice bath under nitrogen and slowly treated with 2N trimethylaluminum in hexane (2.6 eq). After 30 min, the solution was quenched with 3N HCl, diluted with ether and filtered. The organic layer was dried (Na2SO4) and condensed under reduced pressure to afford the crude product. This material was purified by flash silica gel column chromatography using 70% hexane in CH2Cl2. The product was obtained as a colorless oil (80%); MH+ at m/z 172.

후처리

  1. customthe solution was quenched with 3N HCl
  2. additiondiluted with ether
  3. filtrationfiltered
  4. customThe organic layer was dried
  5. custom(Na2SO4) and condensed under reduced pressure
  6. customto afford the crude product
  7. customThis material was purified by flash silica gel column chromatography

출처 및 근거

ORD 기록
ord-378bf1916669437f84ca5c4c053f01c7
출처 데이터셋
uspto-grants-1994_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05294621

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