Pyrrolidine → trans-1,2,3,4-Tetrahydro-2-hydroxy-1-(pyrrolidin-1-yl)naphthalene

HRID 1085480

반응식

HRID 1085480 반응식
[O:1]1[CH:3]2[CH2:4][CH2:5][C:6]3[C:11]([CH:2]12)=[CH:10][CH:9]=[CH:8][CH:7]=3.[NH:12]1[CH2:16][CH2:15][CH2:14][CH2:13]1>C(O)C>[OH:1][C@@H:3]1[CH2:4][CH2:5][C:6]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[C@H:2]1[N:12]1[CH2:16][CH2:15][CH2:14][CH2:13]1

참가 물질

4

실험 절차

A mixture of 1,2-epoxy-1,2,3,4-tetrahydronaphthalene (19.8 g), pyrrolidine (15 ml) and ethanol (75 ml) was stirred at reflux for 2 hours and evaporated of the volatiles under reduced pressure. The residue was dissolved in ether and the solution was extracted with 1N hydrochloric acid (200 ml). The acid extract was washed with ether and basified with 1N sodium hydroxide aqueous solution with cooling. The mixture was extracted with ether (2×) and the combined ether extracts were washed with water, dried over magnesium sulfate and evaporated under reduced pressure. The residual viscous liquid was distilled under vacuum to yield trans-1,2,3,4-tetrahydro-2-hydroxy-1-(pyrrolidin-1-yl)naphthalene (16.5 g), b.p. 128°-135°/0.25 torr.

후처리

  1. temperatureat reflux for 2 hours
  2. customevaporated of the volatiles under reduced pressure
  3. dissolutionThe residue was dissolved in ether
  4. extractionthe solution was extracted with 1N hydrochloric acid (200 ml)
  5. extractionThe acid extract
  6. washwas washed with ether and basified with 1N sodium hydroxide aqueous solution
  7. temperaturewith cooling
  8. extractionThe mixture was extracted with ether (2×)
  9. washthe combined ether extracts were washed with water
  10. dry with materialdried over magnesium sulfate
  11. customevaporated under reduced pressure
  12. distillationThe residual viscous liquid was distilled under vacuum

출처 및 근거

ORD 기록
ord-6ceaba017d0e48a89f3953abaa404cb3
출처 데이터셋
uspto-grants-1991_04
특허 번호
US05010085

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