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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Bromide → 6-Bromo-4-methylpyridin-2-amine

HRID 725751
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HRID 725751 반응식
[C:1]([CH2:3][C:4]([CH3:9])(O)[CH2:5][C:6]#[N:7])#[N:2].[BrH:10]>C(O)(=O)C>[NH2:2][C:1]1[N:7]=[C:6]([Br:10])[CH:5]=[C:4]([CH3:9])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 127207073-Hydroxy-3-methylpentanedinitrile

생성물 1

HCID 221765076-Bromo-4-methylpyridin-2-amine수율 66%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

56.4 g of 1,3-dicyano-2-methyl-2-hydroxypropane was added carefully to a 33% solution of hydrogen bromide in glacial acetic acid at ice-bath temperature. The reaction mixture was then stirred for 3 days at ambient temperature. The solvent was removed in vacuo and the residual oil was brought to pH 12 with a 10 molar aqueous solution of sodium hydroxide. This alkaline solution was extracted three times each with 100 ml ethyl acetate. The combined organic layers were dried with magnesium sulphate and the solvent removed in vacuo. 56 g (66%) of 6-amino-2-bromo-4-methylpyridine was obtained as a colourless solid of melting point 99° C.

후처리

  1. customThe solvent was removed in vacuo
  2. extractionThis alkaline solution was extracted three times each with 100 ml ethyl acetate
  3. dry with materialThe combined organic layers were dried with magnesium sulphate
  4. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-632a4308ac39432e90cd94e0dae25135
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05707933

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