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(4-Carboxybutyl)triphenylphosphonium bromide → HCID 21427638、化合物

HRID 437986
ノート
印刷プレビュー

反応式

HRID 437986 の反応式
[Br-].[C:2]([CH2:5][CH2:6][CH2:7][CH2:8][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([OH:4])=[O:3].[Na].O[CH:30]1[CH2:39][C:38]2[C:33](=[CH:34][CH:35]=[CH:36][CH:37]=2)[CH2:32][O:31]1>CS(C)=O>[OH:31][CH2:32][C:33]1[CH:34]=[CH:35][CH:36]=[CH:37][C:38]=1/[CH:39]=[CH:30]/[CH2:8][CH2:7][CH2:6][CH2:5][C:2]([OH:4])=[O:3]
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 161236(4-Carboxybutyl)triphenylphosphonium bromideHCID 5360545SodiumHCID 12281253Isochroman-3-ol

生成物 1

HCID 21427638HCID 21427638、化合物

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒3 回

実験手順

To a solution of 60.2 g. of 4-carboxybutyltriphenylphosphonium bromide in 200 ml. of dimethylsulfoxide is added a solution of the sodium salt of dimethylsulfoxide. The solution is stirred for one hour and 6.8 g. of 3-hydroxyisochromane in 25 ml. of dimethylsulfoxide is added. The solution is stirred at room temperature for 40 hours and then poured into 1200 ml. of ice water and filtered. The filtrate is washed with ether-ethyl acetate (1:1) and acidified to pH2 with oxalic acid. The mixture is again filtered and the filtrate is extracted with ether-pentane (2:1). The extract is washed with brine, dried, concentrated, and the solid recrystallized from toluene to yield 7-(2-hydroxymethylphenyl)trans-6-heptenoic acid as white crystals having a melting point of 92°-94.5° C.

後処理

  1. stirringThe solution is stirred at room temperature for 40 hours
  2. additionpoured into 1200 ml
  3. filtrationof ice water and filtered
  4. washThe filtrate is washed with ether-ethyl acetate (1:1)
  5. filtrationThe mixture is again filtered
  6. extractionthe filtrate is extracted with ether-pentane (2:1)
  7. washThe extract is washed with brine
  8. customdried
  9. concentrationconcentrated
  10. customthe solid recrystallized from toluene

出典と根拠

ORDレコード
ord-1cef363f2b4f4bc9a86d5dd2fca52bc4
出典データセット
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04032656

反応ノート

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