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Tetrapropoxymethane → 3-Cyano-2-(1,1-dipropoxymethylenamino) thiophene

HRID 1167139
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HRID 1167139 반응식
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][C:6]=1[C:7]#[N:8].[CH2:9]([O:12][C:13](OCCC)(OCCC)[O:14][CH2:15][CH2:16][CH3:17])[CH2:10][CH3:11]>C(O)CC>[C:7]([C:6]1[CH:5]=[CH:4][S:3][C:2]=1[N:1]=[C:13]([O:14][CH2:15][CH2:16][CH3:17])[O:12][CH2:9][CH2:10][CH3:11])#[N:8]
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참가 물질

4

반응물 2

HCID 548455TetrapropoxymethaneHCID 7366072-Aminothiophene-3-carbonitrile

생성물 1

HCID 229958273-Cyano-2-(1,1-dipropoxymethylenamino) thiophene

시약·촉매·용매 1

HCID 10311-Propanol용매

실험 절차

In a small distillation apparatus a mixture of 12.4 g(0.1 mol) 2-amino-3-cyanothiophene and 37.2 g (0.15 mol) tetra-n-propylorthocarbonate is heated for 3 hours at 155° C. n-PrOH, which arises during the reaction is directly distilled out of the reaction flask. After completion of the reaction, excess tetra-n-propylorthocarbonate is distilled off under reduced pressure and the resulting raw material purified by column chromatography over silica gel (eluant: hexane/tert.butylmethyl ether 6:1). Yield: 10.6 g of 3-cyano-2-(1,1-dipropoxymethyleneamino)thiophene in the form of slightly brownish crystals; m.p. 65-67° C.

후처리

  1. distillationis directly distilled out of the reaction flask
  2. customAfter completion of the reaction, excess tetra-n-propylorthocarbonate
  3. distillationis distilled off under reduced pressure
  4. customthe resulting raw material purified by column chromatography over silica gel (eluant: hexane/tert.butylmethyl ether 6:1)

출처 및 근거

ORD 기록
ord-11989f58923544e1b97262d0622e4d2e
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06617330B2

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