Ammonium Chloride → Methyl 8-(p-chlorophenylsulfonamido)-4-[3-(3-pyridyl)-2-propenyl]octanoate

HRID 1494103Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1494103
[Cl-].[N:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:3]=1.CC(C)([O-])C.[K+].[Cl:34][C:35]1[CH:40]=[CH:39][C:38]([S:41]([NH:44][CH2:45][CH2:46][CH2:47][CH2:48][CH:49]([CH2:56][CH:57]=O)[CH2:50][CH2:51][C:52]([O:54][CH3:55])=[O:53])(=[O:43])=[O:42])=[CH:37][CH:36]=1.[Cl-].[NH4+]>O1CCCC1>[Cl:34][C:35]1[CH:36]=[CH:37][C:38]([S:41]([NH:44][CH2:45][CH2:46][CH2:47][CH2:48][CH:49]([CH2:56][CH:57]=[CH:8][C:4]2[CH:3]=[N:2][CH:7]=[CH:6][CH:5]=2)[CH2:50][CH2:51][C:52]([O:54][CH3:55])=[O:53])(=[O:43])=[O:42])=[CH:39][CH:40]=1

Komponenten

6

Edukt 4

HCID 25517Ammonium ChlorideHCID 10340312Methyl 8-(p-chlorophenylsulfonamido)-4-(formylmethyl)octanoateHCID 22325077Triphenyl(3-pyridylmethyl)phosphonium chlorideHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 54073742Methyl 8-(p-chlorophenylsulfonamido)-4-[3-(3-pyridyl)-2-propenyl]octanoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel3×

Versuchsvorschrift

To a suspension of 0.545 g of 3-pyridylmethyltriphenylphosphonium chloride in 6 mL tetrahydrofuran is added slowly 1.6 mL of 1.61 M potassium t-butoxide in tetrahydrofuran and the mixture is stirred at room temperature for 1 hour. A solution of 0.454 g of methyl 8-(p-chlorophenylsulfonamido)-4-(formylmethyl)octanoate in 1 mL tetrahydrofuran is added slowly and then stirred for 18 hours at room temperature. The reaction mixture is poured into saturated ammonium chloride and extracted with ethyl acetate (3×15 mL). The combined organic extracts are dried, filtered and evaporated to give a dark residue which is purified by flash chromatography to obtain, as a light amber oil, methyl 8-(p-chlorophenylsulfonamido)-4-[3-(3- pyridyl)-2-propenyl]-octanoate. The product is a mixture of cis and trans isomers, the major component being the cis isomer. The above product is dissolved in 5 mL methylene chloride in a crystallizing dish and the solution is irradiated for 5 hours under UV light. The organic layer is diluted with methylene chloride and washed with aqueous sodium thiosulfate. The organic phase is dried, filtered and evaporated. The residue is purified by preparative thin layer chromatography to obtain a clear oil identified as about a 1:1 mixture of cis and trans isomers.

Aufarbeitung

  1. stirringstirred for 18 hours at room temperature
  2. extractionextracted with ethyl acetate (3×15 mL)
  3. customThe combined organic extracts are dried
  4. filtrationfiltered
  5. customevaporated
  6. customto give a dark residue which
  7. customis purified by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-f91b062409664becaee1bb4a2dad3185
Quelldatensatz
uspto-grants-1991_06
Patentnummer
US05025025

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