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Sodium Thiosulfate → HCID 131717847, Verbindung

HRID 1589917
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1589917
[O-:1][S:2]([O-:5])(=[S:4])=[O:3].[Na+:6].[Na+].[OH:8]C(C(F)(F)F)=O.[NH2:15][C@H:16]1[CH2:19][O:18][C:17]1=[O:20]>O>[OH2:1].[OH2:8].[Na+:6].[S:2]([S:4][CH2:19][C@@H:16]([C:17]([O-:20])=[O:18])[NH2:15])([OH:5])(=[O:1])=[O:3]
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Komponenten

4

Edukt 2

HCID 24477Sodium ThiosulfateHCID 15600536HCID 15600536, Verbindung

Produkt 1

HCID 131717847HCID 131717847, VerbindungAusbeute 83,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Versuchsvorschrift

To Na2S2O3 (73.2 mg, 0.463 mmol) in H2O (I mL) at pH 5.0 was added (S)-3-amino-2-oxetanone TFA salt (produced from BOC-L-serine β-lactone (43.0 mg, 0.23 mmol)) in H2O (1 mL). The pH was maintained at 5.0 for 1 h and the solvent was removed in vacuo at 25° C. The residue was dissolved in H2O (1.0 mL), applied to a column of Rexyn 102 trademark) (1×10 cm, H+ form) and eluted with (0.25 mL/min). S-sulfo-L-cysteine (Rf 0.81, System A; characteristic brown color with ninhydrin) eluted chromatographically pure as the monosodium salt after 15-20 mL. Lyophilization and recrystallization from H2O/Et2O (pH 5) provided 49.7 mg (83%) of S-sulfo-L-cysteine monosodium salt dihydrate as a white solid: mp 35° C. foams but remains white (loss of H2O), 202°-204° C. (dec); [α]D 25-83.7 (±0.2)° (c 2.5, H2O (lit. [α]D 25 -86.8° (c 4.73, H2O)37 for the 1κ hydrate); IR (KBr disk) 3450 (m, br), 3150 (m, br), 1635 (s, br), 1515 (m), 1400 (m), 1358 (m), 1235 (s), 1217 (s), 1200 (s), 1137 (s), 1030 (s), 636 (s) cm-1 ; 1H NMR (300 MHz, D2O δ 4.18 dd, 1H, 3.7, 8.0 Hz, CH), 3.68 (dd, 1H, 3.7, 15.5 Hz, CHHSSO3-), 3.50 (dd, 1H, 8.0, 15.5 Hz, CHHSSO3-). Anal. Calc. for C3H6NO5S2Na.2H2O (FW 259.2 : C, 13.90; H, 3.89; N, 5.40; S, 24.74. Found: C, 14.11; H, 3.85; N, 5.21; S, 24.59; NEGFAB-MS (glycerol) 200 (-O3SSCH2CH(NH2)COOH).

Aufarbeitung

  1. temperatureThe pH was maintained at 5.0 for 1 h
  2. customthe solvent was removed in vacuo at 25° C
  3. dissolutionThe residue was dissolved in H2O (1.0 mL)
  4. washeluted with (0.25 mL/min)
  5. washS-sulfo-L-cysteine (Rf 0.81, System A; characteristic brown color with ninhydrin) eluted chromatographically pure as the monosodium salt after 15-20 mL
  6. customLyophilization and recrystallization from H2O/Et2O (pH 5)

Quellen und Nachweise

ORD-Eintrag
ord-274c31d915114d47ba852741717e907b
Quelldatensatz
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05200526

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