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Methanesulfonyl chloride → HCID 21993950, Verbindung

HRID 1978369
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1978369
[C:1]([S:4][CH2:5][P:6]([O:11][CH2:12][CH3:13])([O:8][CH2:9][CH3:10])=[O:7])(=O)[CH3:2].C[O-].[Na+].CO.S(OCC1[CH2:30][CH2:29][N:28]([C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[CH2:27][CH2:26]1)(C)(=O)=O.CS(Cl)(=O)=O.OCSCC1CCN(C(OC(C)(C)C)=O)CC1>CO.O1CCCC1.O.C(N(CC)CC)C>[CH2:9]([O:8][P:6]([CH2:5][S:4][CH2:1][CH:2]1[CH2:30][CH2:29][N:28]([C:31]([O:33][C:34]([CH3:36])([CH3:35])[CH3:37])=[O:32])[CH2:27][CH2:26]1)([O:11][CH2:12][CH3:13])=[O:7])[CH3:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 5

HCID 31297Methanesulfonyl chlorideHCID 2765838Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 12536443S-[(Diethoxyphosphoryl)methyl] ethanethioateHCID 21993708HCID 21993708, VerbindungHCID 23694274Sodium methanolate methanol

Produkt 1

HCID 21993950
HCID 21993950, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittelHCID 8471TriethylamineLösungsmittel

Versuchsvorschrift

To a solution of 1.529 g (6.759 mM) of S-(diethoxyphosphorylmethyl) thioacetate in 30 ml of methanol was added 1.30 g (6.76 mM) of 28% sodium methoxide-methanol under ice-cooling and the mixture was stirred at the prevailing temperature for 20 minutes. To this reaction mixture was added crude tert-butyl 4-(mesyloxymethyl)piperidine-1-carboxylate [which was prepared by adding 0.73 ml (9.46 mM) of methanesulfonyl chloride to a solution of 1.75 g (8.11 mM) of tert-butyl 4-(hydroxymethylthiomethyl)piperidine-1-carboxylate and 1.51 ml (10.8 mM) of triethylamine in 30 ml of tetrahydrofuran with ice-cooling, stirring the mixture at the prevailing temperature for 0.5 hour, pouring the mixture in water, extracting it with 2 portions of ethyl acetate, drying the pooled organic layer over MgSO4, and concentrating it], and the mixture was refluxed for 3 hours. The solvent was distilled off under reduced pressure and the residue was diluted with water and extracted with 2 portions of ethyl acetate. The organic layers were pooled and dried over MgSO4 and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate: 3/1 to ethyl acetate) to provide the title compound.

Aufarbeitung

  1. temperaturecooling
  2. customwas prepared
  3. temperaturecooling
  4. stirringstirring the mixture at the prevailing temperature for 0.5 hour
  5. extractionextracting it with 2 portions of ethyl acetate
  6. dry with materialdrying the pooled organic layer over MgSO4
  7. concentrationconcentrating it], and the mixture
  8. temperaturewas refluxed for 3 hours
  9. distillationThe solvent was distilled off under reduced pressure
  10. additionthe residue was diluted with water
  11. extractionextracted with 2 portions of ethyl acetate
  12. dry with materialdried over MgSO4
  13. distillationthe solvent was distilled off under reduced pressure
  14. customThe residue was purified by silica gel column chromatography (hexane-ethyl acetate: 3/1 to ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-cec811c9c7bf4f8eb76c5cd3130d7d9f
Quelldatensatz
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06235731B1

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