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Methyl chloroformate → Methyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate

HRID 2166077
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2166077
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][C@H:2]1[CH2:7][OH:8].Cl[C:10]([O:12][CH3:13])=[O:11].C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C>[OH:8][CH2:7][C@H:2]1[NH:1][CH2:6][CH2:5][N:4]([C:10]([O:12][CH3:13])=[O:11])[CH2:3]1
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Komponenten

5

Edukt 3

HCID 6586Methyl chloroformateHCID 10340Sodium CarbonateHCID 14288866[(2S)-piperazin-2-yl]methanol

Produkt 1

HCID 15645969Methyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylateAusbeute 83,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel2×

Versuchsvorschrift

A solution of the product of stage (ii) (0.080 g) in dry acetonitrile (10 ml) was treated with a solution of methyl chloroformate (71 mg; 0.75 mmol) in dry acetonitrile (3 ml) over a 5 min period. The mixture was stirred at ambient temperature for 30 min and aqueous sodium carbonate solution (1 ml) was added. The solvent was removed in vacuo and the aqueous residue was extracted with dichloromethane (3×25 ml) and chloroform (3×25 ml). The extract was washed with aqueous sodium carbonate solution (5 ml: 1M), and the combined extracts were dried and evaporated in vacuo to give the title compound as an oil (0.1 g).

Aufarbeitung

  1. customThe solvent was removed in vacuo
  2. extractionthe aqueous residue was extracted with dichloromethane (3×25 ml) and chloroform (3×25 ml)
  3. washThe extract was washed with aqueous sodium carbonate solution (5 ml: 1M)
  4. customthe combined extracts were dried
  5. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-680f87e049ae40fea92fa35669932ed9
Quelldatensatz
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04943578

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