4-(4-Chlorothiazol-2-yl)morpholine

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4-(4-Chlorothiazol-2-yl)morpholine Basic information
Product Name:4-(4-Chlorothiazol-2-yl)morpholine
Synonyms:4-(4-Chlorothiazol-2-yl);Morpholine, 4-(4-chloro-2-thiazolyl)-;4-(4-Chlorothiazol-2-yl)morpholine
CAS:848841-68-9
MF:C7H9ClN2OS
MW:204.68
EINECS:
Product Categories:
Mol File:848841-68-9.mol
4-(4-Chlorothiazol-2-yl)morpholine Structure
4-(4-Chlorothiazol-2-yl)morpholine Chemical Properties
Boiling point 327.3±52.0 °C(Predicted)
density 1.388±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka2.31±0.50(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
MSDS Information
4-(4-Chlorothiazol-2-yl)morpholine Usage And Synthesis
Synthesis
Morpholine

110-91-8

2,4-Dichlorothiazole

4175-76-2

4-(4-CHLOROTHIAZOL-2-YL)MORPHOLINE

848841-68-9

A reaction was carried out in acetonitrile (425 mL) with 2,4-dichlorothiazole (34 g, 0.22 mol) and morpholine (21.2 mL, 0.225 mol). Potassium carbonate (60.9 g, 0.44 mol) was first added to the reaction system, followed by slow dropwise addition of morpholine over 30 min. The reaction mixture was refluxed at 40 °C and cooled to 22 °C upon completion. The reaction solution was filtered and the filtrate was evaporated to remove the solvent. The residue was ground with isopropanol (60 mL) at 22 °C for 1 h to promote crystallization. The solid product was collected by filtration and dried under vacuum to constant weight to give the final 4-(4-chlorothiazol-2-yl)morpholine (34.5 g, 76% yield). The product was confirmed by electrospray mass spectrometry (ES/MS), m/z (35Cl) 205 (M + 1)+.

References[1] Patent: WO2008/36579, 2008, A1. Location in patent: Page/Page column 37
[2] Patent: WO2008/83070, 2008, A1. Location in patent: Page/Page column 63
[3] Patent: WO2005/28444, 2005, A1. Location in patent: Page/Page column 73
4-(4-Chlorothiazol-2-yl)morpholine Preparation Products And Raw materials
Raw materialsMorpholine-->2,4-Dichlorothiazole-->Acetonitrile-->Potassium carbonate
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