1. General considerations S1 2. Optimization for oxoammonium salt-mediated nitriles synthesis S2 3. Preparation of aldehydes S2 4. General procedures for 4-AcNH-TEMPO + BF 4 - mediated nitriles synthesis S2 5. Procedure for scale up S7 6. Regeneration of 4-AcNH-TEMPO + BF 4 - S7 7. References S8 8. 1 H and 13 C NMR spectra of substrates S9 Supporting Information for Oxoammonium Salt-Mediated Oxidative Nitriles Synthesis from Aldehydes with Ammonium Acetate Myeong Jin Kim a , Junyoung Mun b,* , Jinho Kim a,* a Department of Chemistry, Incheon National University, 119 Academy-ro, Yeonsu-gu, Incheon 22012, Republic of Korea. [email protected]b Department of Energy and Chemical Engineering, Incheon National University, 119 Academy- ro, Yeonsu-gu, Incheon 22012, Republic of Korea. [email protected]1. General considerations All commercially available compounds and solvents were purchased and used as received, unless otherwise noted. Analytical thin layer chromatography (TLC) was performed on precoated silica gel 60 F254 plates. Visualization on TLC was achieved by the use of UV light (254 nm) and treatment with phosphomolybdic acid stain followed by heating. S1
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ars.els-cdn.com · Web viewThe following abbreviations were used to describe peak splitting patterns when appropriate: br = broad, s = singlet, d = doublet, t = triplet, q = quartet,
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1. General considerations S1
2. Optimization for oxoammonium salt-mediated nitriles synthesis S2
3. Preparation of aldehydes S2
4. General procedures for 4-AcNH-TEMPO+BF4- mediated nitriles synthesis S2
5. Procedure for scale up S7
6. Regeneration of 4-AcNH-TEMPO+BF4- S7
7. References S8
8. 1H and 13C NMR spectra of substrates S9
Supporting Information for
Oxoammonium Salt-Mediated Oxidative Nitriles Synthesisfrom Aldehydes with Ammonium Acetate
Myeong Jin Kima, Junyoung Munb,*, Jinho Kima,*
aDepartment of Chemistry, Incheon National University, 119 Academy-ro, Yeonsu-gu, Incheon 22012, Republic of Korea.
[email protected] of Energy and Chemical Engineering, Incheon National University, 119 Academy-ro,
All commercially available compounds and solvents were purchased and used as received, unless
otherwise noted. Analytical thin layer chromatography (TLC) was performed on precoated silica gel 60
F254 plates. Visualization on TLC was achieved by the use of UV light (254 nm) and treatment with
phosphomolybdic acid stain followed by heating. Flash chromatography was performed using Silica gel
60 (Merck, particle size 40-63 um, 230-400 mesh). 1H and 13C NMR spectra were recorded on Agilent
400 MHz NMR (Agilent Technologies). Chemical shift values are given in parts per million relative to
internal TMS (0.00 ppm for 1H) or CDCl3 (77.06 ppm for 13C). The following abbreviations were used to
describe peak splitting patterns when appropriate: br = broad, s = singlet, d = doublet, t = triplet, q =
quartet, p = pentet, m = multiplet, dd = double of doublet, dt = double of triplet, td = triple of doublet .
Coupling constants, J, were reported in hertz unit (Hz).
2. Optimization for oxoammonium salt-mediated nitriles synthesis
S1
The oxoammnonium salt, 4-AcNH-TEMPO+BF4-, was synthesized according to known procedure.1
A 15 mm flame-dried test tube, which was equipped with a magnetic stir bar and charged with
oxoammonium salt (2.0 equiv, 0.6 mmol) and NH4X (2.4 equiv, 0.72 mmol), was evacuated and
backfilled with nitrogen (this process was repeated 3 times). After 0.3 mL of solvent was added, octanal
(0.3 mmol), and solvent (0.3 mL) were added in sequence. The reaction mixture was stirred for 12 h at 50 oC under N2 balloon, and then cooled to room temperature. The reaction was diluted by adding EtOAc
and washed 4 M HCl aqueous solution. Two layers were separated, and the aqueous layer was extracted
with EtOAc. The combined organic layers were washed with Na2CO3 aqueous solution. The organic
layer was dried over MgSO4, filtered, and concentrated in vacuo. The 1H NMR yield of desired product
was determined by integration using an internal standard (1,1,2,2-tetrachloroethane).
3. Preparation of aldehydes
6-chlorohexanal was prepared by the oxidation of 6-chlorohexanol.2 Adamantane-1-carbaldehyde, 2-
methyl-2-phenylpropanal, and 4-(tert-butyl)cyclohexanecarbaldehyde were prepared from the
corresponding carboxylic acids.3,4 2-Methyl-3-phenylpropanal was prepared by Heck reaction.5 Other
aldehydes are commercially available.
4. General procedures for 4-AcNH-TEMPO+BF4- mediated nitriles synthesis
A 15 mm flame-dried test tube, which was equipped with a magnetic stir bar and charged with aldehyde
(0.3 mmol, in case of solid), 4-AcNH-TEMPO+BF4- (2.0 equiv, 0.6 mmol), and NH4OAc (4.0 equiv, 1.2
mmol), was evacuated and backfilled with nitrogen (this process was repeated 3 times). After 0.3 mL of
AcOH was added, aldehyde (0.3 mmol, in case of liquid), and AcOH (0.3 mL) were added in sequence.
The reaction mixture was stirred for 12 h at 70 oC under N2 balloon, and then cooled to room temperature.
The reaction was diluted by adding EtOAc and washed 4 M HCl aqueous solution. Two layers were
separated, and the aqueous layer was extracted with EtOAc. The combined organic layers were washed
with Na2CO3 aqueous solution. The organic layer was dried over MgSO4, filtered, and concentrated to a
volume of approximately 20 mL by evaporator. To eliminate remaining aldehyde, aqueous 2 M Na2S2O5
aqueous solution (20 mL) was added to the organic layer and stirred for 2 hours. Two layers were
separated, and the organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue
was purified by column chromatography to give nitrile products.