Oxygen → HCID 11784003、化合物

HRID 1585386ノート

反応式

HRID 1585386 の反応式
C(SC=C)=C.C1C(I)=[C:10]([OH:13])C(I)=C2OC3C(C4(OC(=O)C5C(Cl)=C(Cl)C(Cl)=C(Cl)C4=5)C=12)=CC(I)=C(O)C=3I.O=O.FC1C=CC(S[C:49]2([C:62]3[CH:67]=[CH:66][CH:65]=[C:64]([O:68][C:69](=[O:74])[C:70]([CH3:73])([CH3:72])[CH3:71])[CH:63]=3)[C:52]3([CH:59]4[CH2:60][CH:55]5[CH2:56][CH:57]([CH2:61][CH:53]3[CH2:54]5)[CH2:58]4)[O:51][O:50]2)=CC=1.O1CCO1>CO>[CH3:10][O:13][C:49]1([C:62]2[CH:67]=[CH:66][CH:65]=[C:64]([O:68][C:69](=[O:74])[C:70]([CH3:73])([CH3:71])[CH3:72])[CH:63]=2)[C:52]2([CH:53]3[CH2:54][CH:55]4[CH2:56][CH:57]([CH2:58][CH:59]2[CH2:60]4)[CH2:61]3)[O:51][O:50]1

参加物

7

反応物 5

HCID 977OxygenHCID 12321Divinyl sulfideHCID 69439Rose Bengal LactoneHCID 1220291,2-DioxetaneHCID 15327848HCID 15327848、化合物

生成物 1

HCID 11784003HCID 11784003、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

The vinyl sulfide of Example 4(a) (0.051 g) was irradiated in 20 mL of CH3OH containing ca. 1 mg of Rose Bengal with continuous oxygen bubbling at -78° C. using a 1000 W Na lamp. When the alkene was shown by TLC to be completely consumed, iodine (0.096 g) and 1 mL of 30% H2O2 were added and the mixture warmed to room temperature. Progress of the reaction was monitored by the disappearance of dioxetane 4 by TLC (20% ethyl acetate in hexane) and the appearance of new bands which emitted blue light when the plate was heated and by observing the color of chemiluminescence from an aliquot of the reaction solution reacted with 0.1 M TBAF in DMSO. The yellow emission of dioxetane 4 was gradually replaced by the blue emission of dioxetane 20 over a period of two hours. The solution was concentrated to 1-2 mL and separated on preparative TLC with 5% ethyl acetate in hexane. The band containing dioxetane 20 was collected and desorbed and evaporated to yield the product as a slightly yellow oil: 1H NMR (CDCl3) δ1.02 (m, 1H), 1.28 (m, 1H), 1.375 (s, 9H), 1.45-1.94 (m, 10H), 2.17 (br s, 1H), 3.04 (br s, 1H), 3.232 (s, 3H), 7.07-7.49 (m, 4H).

後処理

  1. customto be completely consumed
  2. additioniodine (0.096 g) and 1 mL of 30% H2O2 were added
  3. temperaturewas heated
  4. customreacted with 0.1 M TBAF in DMSO
  5. concentrationThe solution was concentrated to 1-2 mL
  6. customseparated on preparative TLC with 5% ethyl acetate in hexane
  7. additionThe band containing dioxetane 20
  8. customwas collected
  9. customevaporated
  10. customto yield the product as a slightly yellow oil

出典と根拠

ORDレコード
ord-1a2a24e3a13b4dc5afaafb9ee55f82e4
出典データセット
uspto-grants-1999_08
特許番号
US05936101

反応ノート

読み込み中…