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Sodium Hydroxide → Carbamic acid, [2-chloro-2-(3-thienyl)ethyl]-, 1,1-dimethylethyl ester

HRID 256052
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 256052
[C:1]([O:5][C:6]([NH:8][CH2:9][CH:10]([C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)O)=[O:7])([CH3:4])([CH3:3])[CH3:2].P(Cl)(Cl)(Cl)(Cl)[Cl:18].[OH-].[Na+]>C(Cl)Cl>[C:1]([O:5][C:6]([NH:8][CH2:9][CH:10]([Cl:18])[C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 14798Sodium HydroxideHCID 24819Phosphorus pentachlorideHCID 13854065HCID 13854065, Verbindung

Produkt 1

HCID 13854066Carbamic acid, [2-chloro-2-(3-thienyl)ethyl]-, 1,1-dimethylethyl esterAusbeute 55,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a solution of 12.2 g of 2-t-butoxycarbonylamino-1-(3-thienyl)ethanol [prepared as described in step (a) above] in 100 ml of absolute methylene chloride was added a solution of 10.4 g of phosphorus pentachloride in 200 ml of absolute methylene chloride at 0° to -5° C. After the addition, the reaction mixture was stirred for 10 minutes. To the reaction mixture was added a 4N aqueous solution of sodium hydroxide, and the mixture was stirred for 5 minutes. The methylene chloride layer was separated, washed with large amount of water and dried over anhydrous magnesium sulfate, and the solvent was evaporated off. The residue was subjected to silica gel column chromatography using a 1:4 by volume mixture of ethyl acetate and cyclohexane as eluent, to yield 7.3 g of the title compound melting at 63°-65° C.

Aufarbeitung

  1. additionAfter the addition
  2. stirringthe mixture was stirred for 5 minutes
  3. customThe methylene chloride layer was separated
  4. washwashed with large amount of water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated off
  7. additionby volume mixture of ethyl acetate and cyclohexane as eluent

Quellen und Nachweise

ORD-Eintrag
ord-e78819c6aac74ed4a4d4ab8edcbe1a30
Quelldatensatz
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04699905

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