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Hydrogen Bromide → (1S)-2-methyl-2,5-diazobicyclo[2.2.1]heptane dihydrobromide

HRID 1614346
ノート
印刷プレビュー

反応式

HRID 1614346 の反応式
C1(C)C=CC(S([N:10]2[CH2:15][C@@H:14]3[CH2:16][C@H:11]2[CH2:12][N:13]3[CH3:17])(=O)=O)=CC=1.[BrH:19]>C(O)(=O)C>[BrH:19].[BrH:19].[CH3:17][N:13]1[CH2:12][C@@H:11]2[CH2:16][C@H:14]1[CH2:15][NH:10]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 260Hydrogen BromideHCID 11054620(1S,4S)-2-Methyl-5-tosyl-2,5-diazabicyclo[2.2.1]heptane

生成物 1

HCID 15629279(1S)-2-methyl-2,5-diazobicyclo[2.2.1]heptane dihydrobromide収率 81%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

60 g (225 mmol) of (1S, 4S)-2-(4-Toluenesulfonyl)-5-methyl-2,5-diazabicyclo-[2.2.1]heptane was suspended in 900 ml of 30% hydrogen bromide in acetic acid and the mixture was allowed to stir at room temperature. After 6 hours the acetic acid was removed under aspirator pressure to 1/4 of the original volume and 1800 ml of ethylacetate was then added. A solid precipitated and was filtered under an inert atmosphere. The product was recrystallized by dissolving in a minimum amount of methanol at reflux. Cooling followed by the addition of 400 ml of isopropyl alcohol provided a white solid which was filtered and dried under reduced pressure. The product weighed 48 g which represents an 81% yield. M.P.=258°-259° C. (coloration occurs at 234° C.). [α]D =+13.21° (c=0.946, CH3OH)

後処理

  1. customAfter 6 hours the acetic acid was removed under aspirator pressure to 1/4 of the original volume and 1800 ml of ethylacetate
  2. additionwas then added
  3. customA solid precipitated
  4. filtrationwas filtered under an inert atmosphere
  5. customThe product was recrystallized
  6. dissolutionby dissolving in a minimum amount of methanol
  7. temperatureat reflux
  8. temperatureCooling
  9. additionfollowed by the addition of 400 ml of isopropyl alcohol
  10. customprovided a white solid which
  11. filtrationwas filtered
  12. customdried under reduced pressure
  13. customM.P.=258°-259° C. (coloration occurs at 234° C.)
  14. custom[α]D =+13.21° (c=0.946, CH3OH)

出典と根拠

ORDレコード
ord-f7bffaca204b4c22a0ebcd10eaf73614
出典データセット
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05196548

反応ノート

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