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Ozone → HCID 28562535、化合物

HRID 55446
ノート
印刷プレビュー

反応式

HRID 55446 の反応式
[O:1]=[O+][O-].[CH2:4]([O:7][C:8]1[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=1[CH2:10][OH:11])[CH:5]=C.[BH4-].[Na+]>CO>[OH:1][CH2:5][CH2:4][O:7][C:8]1[CH:15]=[CH:14][CH:13]=[CH:12][C:9]=1[CH2:10][OH:11]
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 24823OzoneHCID 4311764Sodium borohydrideHCID 11137475[2-(Allyloxy)phenyl]methanol

生成物 1

HCID 28562535HCID 28562535、化合物収率 67%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Ozone was bubbled through a -78° C. dry methanol solution of 2-(allyloxy)benzyl alcohol (LaChapelle et al Tetrahedron, 44(16), 5033-5044 (1988)) (7.0 g, 43 mmol) for 13 minutes, checking the reaction TLC profile every 2 minutes for complete disappearance of the starting olefin (Rf=0.8, 75% EtOAc/hexane). The reaction mixture was purged with nitrogen, NaBH4 (9.7 g, 0.25 mol) was added and the reaction temperature brought to 0° C. After 30 minutes, the reaction was warmed to room temperature, concentrated, diluted with ether, washed with water, brine, dried and concentrated to a residue. The residue was eluted through a pad of silica with EtOAc/hexanes (gradient elution 25%-75% EtOAC). Evaporation of the eluting solvent gave the diol, 2-(2'-hydroxyethoxy)-benzyl alcohol, (4.8 g, 67%) as an oil. MS: MW=168; observed 168, FD, CHCl3).

後処理

  1. customthe reaction
  2. additionwas added
  3. custombrought to 0° C
  4. concentrationconcentrated
  5. additiondiluted with ether
  6. washwashed with water, brine
  7. customdried
  8. concentrationconcentrated to a residue
  9. washThe residue was eluted through a pad of silica with EtOAc/hexanes (gradient elution 25%-75% EtOAC)
  10. customEvaporation of the eluting solvent

出典と根拠

ORDレコード
ord-10d26b49776d437783ffb13e57d65c51
出典データセット
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05624949

反応ノート

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