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1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 56594895、化合物

HRID 2219871
ノート
印刷プレビュー

反応式

HRID 2219871 の反応式
[CH3:1][O:2][C:3]([C:5]1[CH:14]=[CH:13][C:12]2[C@@H:11](O)[CH2:10][CH2:9][CH2:8][C:7]=2[CH:6]=1)=[O:4].C1C=CC(P([N:30]=[N+:31]=[N-:32])(C2C=CC=CC=2)=O)=CC=1.C1CCN2C(=NCCC2)CC1>C1(C)C=CC=CC=1>[N:30]([C@@H:11]1[CH2:10][CH2:9][CH2:8][C:7]2[CH:6]=[C:5]([C:3]([O:2][CH3:1])=[O:4])[CH:14]=[CH:13][C:12]1=2)=[N+:31]=[N-:32]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 199401P,P-Diphenylphosphinic azideHCID 56594894methyl (S)-5-hydroxy-5,6,7,8-tetrahydronaphthalene-2-carboxylate

生成物 1

HCID 56594895HCID 56594895、化合物

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a 500 mL three-neck round-bottomed flask equipped with argon inlet/outlet, thermometer, and magnetic stirring was added 5(S)-hydroxy-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid methyl ester (29 g, 140 mmol) in 280 mL of toluene. The reaction mixture was cooled in a ice-salt bath, and DPPA (36 mL, 170 mmol, Aldrich) was added (internal temp.=−4° C.). DBU (25 mL, 170 mmol, Aldrich) was added over 10 min at such a rate that the internal temperature was kept below 1° C. The ice in the bath was allowed to melt, and the reaction continued for 12 h during which time the mixture stopped stirring because a precipitate had formed. Stirring was resumed, and the reaction mixture was stirred at RT for another 11 h. The reaction contents were poured into a 2 L sep funnel, and the lower dark-brown layer was removed. Water (250 mL) was added to the remaining top layer, and the mixture was extracted with Et2O (3×250 mL). The combined organic layers were washed with 1M H3PO4, water, satd NaHCO3, and brine. The organic layer was dried over MgSO4, filtered and concentrated in vacuo. Purification by silica gel chromatography (330 g Isco Redisep® column, 1:1 hexane-CH2Cl2) of the crude material provided the title compound. MS (+ion ESI) m/z =232 (MH+).

後処理

  1. customTo a 500 mL three-neck round-bottomed flask equipped with argon inlet/outlet
  2. temperatureThe reaction mixture was cooled in a ice-salt bath
  3. customwas kept below 1° C
  4. stirringthe mixture stopped stirring because a precipitate
  5. customhad formed
  6. stirringStirring
  7. stirringthe reaction mixture was stirred at RT for another 11 h
  8. customThe reaction contents
  9. additionwere poured into a 2 L sep funnel
  10. customthe lower dark-brown layer was removed
  11. additionWater (250 mL) was added to the remaining top layer
  12. extractionthe mixture was extracted with Et2O (3×250 mL)
  13. washThe combined organic layers were washed with 1M H3PO4, water
  14. dry with materialThe organic layer was dried over MgSO4
  15. filtrationfiltered
  16. concentrationconcentrated in vacuo
  17. customPurification by silica gel chromatography (330 g Isco Redisep® column, 1:1 hexane-CH2Cl2) of the crude material

出典と根拠

ORDレコード
ord-2842a62e934d47809034d12fdc6bb295
出典データセット
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07414134B2

反応ノート

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