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Hydrogen Peroxide → HCID 131716835、化合物

HRID 1085924
ノート
印刷プレビュー

反応式

HRID 1085924 の反応式
[O:1]1[CH2:5][C:4](=[O:6])[N:3]=[C-:2]1.[O-]S(C(F)(F)F)(=O)=O.C([B+]CCCC)CCC.COC1C=C[C:29]([CH2:30][O:31][CH2:32][CH2:33]C=O)=CC=1.P([O-])([O-])([O-])=O.OO>C(Cl)Cl.C(N(CC)CC)C>[O:1]1[CH2:5][C:4](=[O:6])[N:3]=[C-:2]1.[CH3:29][CH2:30][O:31][CH2:32][CH3:33]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 784Hydrogen PeroxideHCID 1061PhosphateHCID 10997887Propanal, 3-[(4-methoxyphenyl)methoxy]-HCID 532495662H-1,3-oxazol-2-id-4-oneHCID 178418657HCID 178418657、化合物

生成物 1

HCID 131716835HCID 131716835、化合物

試薬・触媒・溶媒 2

HCID 6344
Dichloromethane
溶媒
3 回
HCID 8471Triethylamine溶媒

反応条件

温度
0 °C

実験手順

To a solution of 3.21 g of the oxazolidone 15 in 40 ml of methylene chloride at -78° C. was added 13.64 ml of a 1M dibutylboron triflate in methylene chloride solution and 2.6 ml of triethylamine. The reaction solution was stirred at 0° C. for 30 minutes, then it was cooled to -78° C. 3-(4-Methoxybenzyloxy)propanaldehyde (2.4 g) in 4 ml of methylene chloride was added and the reaction solution was stirred 30 minutes at -78° C. and then at RT for 1.5 hour. At the end of this time 100 ml of pH7 phosphate buffer was added, followed by addition of 30% aqueous hydrogen peroxide to the mixture at 0° C. The mixture was then extracted twice with diethyl ether and the aqueous phases were dried with sodium sulfate. The solution was concentrated under vacuum and chromatography of the residue over silica gel (2 hexanes: 1 EtOAc) provided the title compound.

後処理

  1. temperatureit was cooled to -78° C
  2. stirringthe reaction solution was stirred 30 minutes at -78° C.
  3. waitat RT for 1.5 hour
  4. extractionThe mixture was then extracted twice with diethyl ether
  5. dry with materialthe aqueous phases were dried with sodium sulfate
  6. concentrationThe solution was concentrated under vacuum and chromatography of the residue over silica gel (2 hexanes: 1 EtOAc)

出典と根拠

ORDレコード
ord-4d13c309a9c844378dcbee9b1c0f0daf
出典データセット
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05011943

反応ノート

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