4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide

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4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide manufacturers

4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide Basic information
Product Name:4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide
Synonyms:2-(1,1-DIOXOTHIOMORPHOLINO)ETHANOL;N-(2-HYDROXYETHYL) THIOMORPHOLINE 1,1-DIOXIDE;4-THIOMORPHOLINEETHANOL-1-DIOXIDE;1-DIXOIDE-4-THIOMORPHOLINEETHANOL;1-DIOXIDE-4-THIOMORPHOLINEETHANOL;4-(2-hydroxyethyl)-1$l^{6},4-thioMorpholine-1,1-dione;EOS-60875;2-(1,1-DIOXO-1,4-THIAZINAN-4-YL)ETHANOL
CAS:26475-62-7
MF:C6H13NO3S
MW:179.24
EINECS:
Product Categories:
Mol File:26475-62-7.mol
4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide Structure
4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide Chemical Properties
Melting point 74 °C
Boiling point 197 °C / 1mmHg
density 1.287±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Methanol
form powder to crystal
pka14.80±0.10(Predicted)
color White to Light yellow to Light orange
InChIInChI=1S/C6H13NO3S/c8-4-1-7-2-5-11(9,10)6-3-7/h8H,1-6H2
InChIKeyGILLKIJFJOBJCD-UHFFFAOYSA-N
SMILESN1(CCO)CCS(=O)(=O)CC1
CAS DataBase Reference26475-62-7(CAS DataBase Reference)
Safety Information
HS Code 2934999090
MSDS Information
4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide Usage And Synthesis
Synthesis
Thiomorpholine-1,1-dioxide

39093-93-1

2-Bromoethanol

540-51-2

4-(2-HYDROXYETHYL)THIOMORPHOLINE 1,1-DIOXIDE

26475-62-7

To a stirred solution of 2-bromoethanol (11.78 mL, 165.92 mmol, 7.0 equiv) in acetonitrile (68 mL) was added potassium carbonate (9.8 g, 71.10 mmol, 3.0 equiv). The reaction mixture was stirred at room temperature for 30 minutes before thiomorpholine-1,1 -dioxide (3.2 g, 23.70 mmol, 1.0 eq.) was added. The reaction mixture was heated to reflux and stirred overnight. The progress of the reaction was monitored by thin layer chromatography (TLC) to confirm that the feedstock was completely consumed and the target product was generated. Upon completion of the reaction, the mixture was cooled to room temperature and filtered. The filtrate was concentrated to obtain the crude product, which was subsequently purified by column chromatography using a mixture of dichloromethane and 3% methanol as eluent, resulting in 4-(2-hydroxyethyl)thiomorpholine-1,1-dioxide (2.5 g, 60.0% yield) as a brown liquid. The product was characterized by 1H NMR (DMSO-d6, 300 MHz): δ 4.50 (t, 1H), 3.51 (q, 2H), 3.07 (m, 4H), 2.95 (m, 4H), 2.58 (t, 2H); Mass Spectrometry (MS): [M + H]+ m/z 180.19 (10%).

References[1] Patent: WO2017/149518, 2017, A1. Location in patent: Page/Page column 24; 25
4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide Preparation Products And Raw materials
Raw materialsThiomorpholine-1,1-dioxide-->2-Bromoethanol-->Acetonitrile-->Potassium carbonate
Tag:4-(2-Hydroxyethyl)thiomorpholine 1,1-dioxide(26475-62-7) Related Product Information
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