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Cysteamine Hydrochloride → 2-((Thiophen-2-ylmethyl)thio)ethan-1-amine

HRID 224862
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 224862
Cl.[NH2:2][CH2:3][CH2:4][SH:5].O[CH2:7][C:8]1[S:9][CH:10]=[CH:11][CH:12]=1.[OH-].[Na+]>Cl>[S:9]1[CH:10]=[CH:11][CH:12]=[C:8]1[CH2:7][S:5][CH2:4][CH2:3][NH2:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 9082Cysteamine HydrochlorideHCID 14798Sodium HydroxideHCID 694672-Thiophenemethanol

Produkt 1

HCID 49622502-((Thiophen-2-ylmethyl)thio)ethan-1-amine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 313Hydrochloric AcidLösungsmittel

Versuchsvorschrift

(b)(i) Cysteamine hydrochloride (9.95 g) was dissolved in concentrated hydrochloric acid (50 ml) and the solution was cooled to 0°. 2-Hydroxymethylthiophene (10 g) was added dropwise to the stirred solution which was maintained at below 5°. The mixture was stirred overnight at room temperature, adjusted to pH 10 with concentrated aqueous sodium hydroxide and extracted with ethyl acetate. The extracts were evaporated and the residue was distilled at 158°-164°/760 mm Hg to give 2-(2-thienylmethylthio)ethylamine which was converted into the hydrochloride, m.p. 108°-111°, by treatment with ethanolic HCl and ether.

Aufarbeitung

  1. temperaturethe solution was cooled to 0°
  2. temperaturewas maintained at below 5°
  3. extractionextracted with ethyl acetate
  4. customThe extracts were evaporated
  5. distillationthe residue was distilled at 158°-164°/760 mm Hg

Quellen und Nachweise

ORD-Eintrag
ord-3b56b78cdbd94d0a86b58353a969bcad
Quelldatensatz
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04234588

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