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2-Fluoroethyl 4-methylbenzenesulfonate

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2-Fluoroethyl 4-methylbenzenesulfonate manufacturers

2-Fluoroethyl 4-methylbenzenesulfonate Basic information
Product Name:2-Fluoroethyl 4-methylbenzenesulfonate
Synonyms:Fluoroethylp-tosylate;2-Fluoro-(4-methylbenzenesulfonate)ethanol;FLUOROETHYL 4-TOLUENESULFONATE;L-TRYPTOPHAN/D-TRYPTOPHAN;2-fluoroethyl 4-methylbenzenesulfonate;Fluoroethyl p-toluenesulfonate;4-Methylbenzenesulfonic acid 2-fluoro-ethyl ester;2-fluoroethyl 4-Methylbenzene-1-sulfonate
CAS:383-50-6
MF:C9H11FO3S
MW:218.25
EINECS:
Product Categories:
Mol File:383-50-6.mol
2-Fluoroethyl 4-methylbenzenesulfonate Structure
2-Fluoroethyl 4-methylbenzenesulfonate Chemical Properties
Boiling point 140°C/1mmHg(lit.)
density 1.290 g/cm3
refractive index 1.5060 to 1.5100
Fp > 70 °C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Oil
color Clear Colourless to Pale Brown
InChIInChI=1S/C9H11FO3S/c1-8-2-4-9(5-3-8)14(11,12)13-7-6-10/h2-5H,6-7H2,1H3
InChIKeyXNRDLSNSMTUXBV-UHFFFAOYSA-N
SMILESC(OS(C1=CC=C(C)C=C1)(=O)=O)CF
CAS DataBase Reference383-50-6(CAS DataBase Reference)
Safety Information
HS Code 2930909899
MSDS Information
2-Fluoroethyl 4-methylbenzenesulfonate Usage And Synthesis
Uses2-Fluoroethyl Tosylate is an intermediate used in the preparation and pre-clinical evaluation of new class of high-affinity 18F-labeled PSMA ligands for detection of prostate cancer by positron emission tomography (PET) imaging.
Synthesis
2-Fluoroethanol

371-62-0

Tosyl chloride

98-59-9

2-Fluoroethyl 4-methylbenzenesulfonate

383-50-6

2-Fluoroethanol (1.00 mL, 16.9 mmol), p-toluenesulfonyl chloride (3.85 g, 20.2 mmol), N-methylmorpholine (9.30 mL, 84.5 mmol), and dichloromethane (50 mL) were added to the reaction vessel, and the reaction was stirred for 17 hours at room temperature. After completion of the reaction, water was added to the reaction system and extracted with ethyl acetate three times to combine the organic layers. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, the residue was purified by fast silica gel column chromatography (eluent: ethyl acetate/hexane=19:81→40:60) to afford fluoroethyl p-toluenesulfonate (3.79 g, 17.2 mmol, yield >100%) as a pale yellow liquid.1H NMR (600 MHz, CDCl3): δ 7.81 (d, J=8.4 Hz, 2H), δ 7.36 (d, J=8.4 Hz, 2H), 4.63-4.60 (m, 1H), 4.55-4.52 (m, 1H), 4.31-4.27 (m, 1H), 4.26-4.23 (m, 1H), 2.46 (s, 3H). lRMS (EI) Calculated value (C9H11F3O): 218.0, measured value: 218.0.

References[1] Patent: US2018/30074, 2018, A1. Location in patent: Paragraph 0188-0191
[2] Journal of Labelled Compounds and Radiopharmaceuticals, 2008, vol. 51, # 7, p. 286 - 292
[3] Patent: US2013/177501, 2013, A1. Location in patent: Paragraph 0168
[4] Patent: US9168317, 2015, B2. Location in patent: Page/Page column 25; 26
[5] Patent: US9314541, 2016, B2. Location in patent: Page/Page column 26
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