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Methanol → Thionyl Chloride

HRID 263841
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 263841
[S:1]([Cl:4])([Cl:3])=[O:2].[NH2:5][C@@H:6]([CH2:10][NH2:11])[C:7]([OH:9])=[O:8].[CH3:12]O>>[S:1]([Cl:4])([Cl:3])=[O:2].[ClH:3].[NH2:5][C@@H:6]([CH2:10][NH2:11])[C:7]([O:9][CH3:12])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 887Methanol2×HCID 24386Thionyl ChlorideHCID 97328L-alpha,beta-Diaminopropionic acid

Produkt 2

HCID 24386Thionyl ChlorideHCID 22852130HCID 22852130, Verbindung

Versuchsvorschrift

Methanol (400 mL) was cooled to 0° C. and thionyl chloride (217 mL, 3.0 moles, 20 eq) was added dropwise under argon. After addition was completed, the solution was warmed to RT for 20 min. 2(S),3-Diaminopropanoic acid 2-1 (20 g, 0.143 mole) (Schweizerhall Chemicals) was crushed to a fine powder and added to the solution. The reaction was heated to reflux for 48 h, at which time TLC showed a small amount of starting material remaining. An additional portion of methanol (100 mL) and thionyl chloride (72 mL) was prepared as before and added to the reaction at RT; the reaction was then stirred overnight at RT. The reaction was worked up by removal of solvent at 40° C. in vacuo to give 2-2 as foam. Rf 0.72 (9:1:1 EtOH/H2O/NH4OH). 1H NMR (400 MHz, D2O) δ4.55 (dd, J=5.4 8.2 Hz, 1H), 3.92 (s, 3H), 3.64 (dd, J=8.2, 13.8 Hz, 1H), 3.55 (dd, J=5.4, 13.8 Hz, 1H).

Aufarbeitung

  1. additionAfter addition
  2. additionadded to the solution
  3. temperatureThe reaction was heated
  4. temperatureto reflux for 48 h, at which time TLC
  5. additionadded to the reaction at RT
  6. customThe reaction was worked up by removal of solvent at 40° C. in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-1c0106c52e924777920c0772a1de0fbe
Quelldatensatz
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05646000

Notizen zur Reaktion

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