p-Toluenesulfonic acid → Pentanoic acid, 5-(triphenylphosphoranylidene)-

HRID 1448657Notes

Reaction equation

HRID 1448657 reaction equation
O1C=CCCC1.O1C=CCC1.C(OCC)=C.C1(C)C=CC(S(O)(=O)=O)=CC=1.[H-].C([Al+]CC(C)C)C(C)C.[H-].[Na+].[Br-].[C:41]([CH2:44][CH2:45][CH2:46][CH2:47][P+:48]([C:61]1[CH:66]=[CH:65][CH:64]=[CH:63][CH:62]=1)([C:55]1[CH:60]=[CH:59][CH:58]=[CH:57][CH:56]=1)[C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1)([OH:43])=[O:42]>C1(C)C=CC=CC=1.CS(C)=O.C(Cl)Cl>[C:41]([CH2:44][CH2:45][CH2:46][CH:47]=[P:48]([C:61]1[CH:66]=[CH:65][CH:64]=[CH:63][CH:62]=1)([C:49]1[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=1)[C:55]1[CH:60]=[CH:59][CH:58]=[CH:57][CH:56]=1)([OH:43])=[O:42]

Participants

11

Procedure

Compounds of formula XX may be prepared by hydrolysis under alkaline conditions of compounds of formula XIX. Compounds of formula XXI may be obtained by the acetylation of compounds of formula XX under mild conditions and may be converted into compounds of formula XXII by reaction with a dihydropyran, dihydrofuran or ethyl vinyl ether in an inert solvent, e.g. methylene chloride, in the presence of a condensing agent, e.g. p-toluenesulphonic acid. Compounds of formula XXIII may be prepared by reducing compounds of formula XXII with diisobutylaluminium hydride in toluene for about 15 minutes at -60° C. Dimsyl anion, previously prepared from sodium hydride and dimethyl sulphoxide, is reacted with (4-carboxybutyl)triphenylphosphonium bromide to form (4-carboxybutylidene)triphenylphosphorane. To that compound is added a compound of formula XXIII and the mixture in dimethyl sulphoxide is made to react for 2 hours at room temperature to yield a compound of formula XVA.

Workup

  1. customfor about 15 minutes
  2. customat -60° C

Sources & evidence

ORD record
ord-b577f55d9b264de8ab5638b1c255afc1
Source dataset
uspto-grants-1979_12
Patent number
US04180675

Reaction notes

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