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Potassium Hydroxide → 3-bromo-6,7,8,9-tetrahydro-5H-10-thia-7-aza-benzo[a]azulene

HRID 271696
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HRID 271696 반응식
[OH-].[K+].[Br:3][C:4]1[CH:5]=[CH:6][C:7]2[S:16][C:15]3[CH2:14][CH2:13][N:12](C(OCC)=O)[CH2:11][CH2:10][C:9]=3[C:8]=2[CH:22]=1>CCO>[Br:3][C:4]1[CH:5]=[CH:6][C:7]2[S:16][C:15]3[CH2:14][CH2:13][NH:12][CH2:11][CH2:10][C:9]=3[C:8]=2[CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 69079455Ethyl 3-bromo-5,6,8,9-tetrahydro-10-thia-7-aza-benzo[a]azulen-7-carboxylate

생성물 1

HCID 673642873-bromo-6,7,8,9-tetrahydro-5H-10-thia-7-aza-benzo[a]azulene

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

30.0 g (53.5 mmol) KOH in 700 mL EtOH are added to a solution of 19.0 g (53.5 mmol) ethyl 3-bromo-5,6,8,9-tetrahydro-10-thia-7-aza-benzo[a]azulen-7-carboxylate. EtOH is distilled off at normal pressure and the residue is taken up in water. The solution is acidified with HCl. Then it is made basic with NaOH and the aqueous phase is extracted four times with chloroform. The organic phase is dried over Na2SO4 and K2CO3 and the solvent is eliminated i.vac. The purification is carried out by repeated column chromatography on silica gel.

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후처리

  1. distillationEtOH is distilled off at normal pressure
  2. extractionthe aqueous phase is extracted four times with chloroform
  3. dry with materialThe organic phase is dried over Na2SO4 and K2CO3
  4. customThe purification

출처 및 근거

ORD 기록
ord-5d613efc1a91423484a71d7d78ac9e5d
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452911B2

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