Conditions | Yield |
---|---|
With potassium carbonate | |
Versetzen mit 40prozentiger KOH; | |
With potassium carbonate |
acetamide
formaldehyd
A
N,N-methylenediacetamide
B
N-(hydroxymethyl)acetamide
Conditions | Yield |
---|---|
In 1,4-dioxane; water at 40 - 60℃; Thermodynamic data; Kinetics; Mechanism; activation energy, pH 1.2-3.5; |
Conditions | Yield |
---|---|
In water Mechanism; Quantum yield; Irradiation; neutral solution; |
glycylglycine
A
acetamide
B
N,N-methylenediacetamide
C
N-(hydroxymethyl)acetamide
D
N-acetylglycine
Conditions | Yield |
---|---|
In water Product distribution; Quantum yield; Mechanism; Irradiation; pH 6; var. dipeptides, other pH and times; |
3,7-diacetyl-1,3,5,7-tetraaza-bicyclo[3.3.1]nonane
A
formaldehyd
B
N-(hydroxymethyl)acetamide
Conditions | Yield |
---|---|
With hydrogenchloride In water at 25℃; for 0.333333h; | A 1.7 % Turnov. B n/a |
Conditions | Yield |
---|---|
at 120 - 150℃; |
6-methyl-2-p-tolyl-imidazo[1,2-a]pyridin-4-ium bromide
N-(hydroxymethyl)acetamide
C18H19N3O
Conditions | Yield |
---|---|
Stage #1: 6-methyl-2-p-tolyl-imidazo[1,2-a]pyridin-4-ium bromide; N-(hydroxymethyl)acetamide With sulfuric acid In acetic acid at 20℃; for 3.5h; Heating / reflux; Stage #2: With ammonia In water; acetic acid | 97% |
N-(hydroxymethyl)acetamide
5,17-dibromo-25,27-bis(2-ethoxyethoxy)calix[4]arene
Conditions | Yield |
---|---|
With trifluoroacetic acid In chloroform Ambient temperature; | 95% |
2-mercapto-4,5-dimethoxybenzylamine hydrochloride
N-(hydroxymethyl)acetamide
Conditions | Yield |
---|---|
With hydrogenchloride | 94% |
Conditions | Yield |
---|---|
With sulfuric acid In ethanol at 35℃; for 96h; Friedel-Crafts Alkylation; | 91.36% |
N-(hydroxymethyl)acetamide
6-benzylthio-2-phenethylimidazo<1,2-b>pyridazine
3-acetamidomethyl-6-benzylthio-2-phenethylimidazo<1,2-b>pyridazine
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid Heating; | 90% |
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid for 14h; Heating; | 90% |
Conditions | Yield |
---|---|
With sulfuric acid In ethanol at 35℃; for 96h; Friedel-Crafts Alkylation; | 89.68% |
N-(hydroxymethyl)acetamide
25,27-dihydroxy-26,28-dipropoxycalix[4]arene
Conditions | Yield |
---|---|
With trifluoroacetic acid In chloroform Ambient temperature; | 85% |
N-(hydroxymethyl)acetamide
6-(2-Methoxy-phenylsulfanyl)-2-phenyl-imidazo[1,2-b]pyridazine
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid at 100℃; for 14h; | 83% |
N-(hydroxymethyl)acetamide
5,17-dibromo-25,26,27,28-tetra-n-propylcalix[4]arene
Conditions | Yield |
---|---|
With trifluoroacetic acid In chloroform for 36h; Ambient temperature; | 83% |
N-(hydroxymethyl)acetamide
2-Benzo[1,3]dioxol-5-yl-6-chloro-imidazo[1,2-b]pyridazine
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid for 14h; Heating; | 80% |
N-(hydroxymethyl)acetamide
2-(4'-methylphenyl)-6-phenylthioimidazo<1,2-b>pyridazine
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid for 14h; Heating; | 80% |
N-(hydroxymethyl)acetamide
Conditions | Yield |
---|---|
With trifluoroacetic acid at 20℃; for 0.166667h; | 79% |
Conditions | Yield |
---|---|
With sulfuric acid In ethanol at 35℃; for 96h; Friedel-Crafts Alkylation; | 78.55% |
2-mercaptopropanoic acid
N-(hydroxymethyl)acetamide
(RS)-2-acetamidomethylthiopropionic acid
Conditions | Yield |
---|---|
With trifluoroacetic acid for 0.75h; Ambient temperature; | 78% |
N-(hydroxymethyl)acetamide
2-(4'-t-butylphenyl)-6-chloroimidazo<1,2-b>pyridazine
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid for 14h; Heating; | 74% |
11-mercaptounadecanoic acid
N-(hydroxymethyl)acetamide
Conditions | Yield |
---|---|
In trifluoroacetic acid for 0.5h; Ambient temperature; | 72% |
3,3-dimethyl-D-cysteine
N-(hydroxymethyl)acetamide
bis(S)(-5,5-dimethylthiazolidine-4-carboxylic acid)protium chloride hydrate
Conditions | Yield |
---|---|
With hydrogenchloride In water for 0.5h; Ambient temperature; | 70% |
2-amino-2-(1-mercaptocyclopentyl)acetic acid hydrochloride
N-(hydroxymethyl)acetamide
trifluoroacetic acid
C2HF3O2*C10H18N2O3S
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid In water at 0 - 20℃; | 70% |
N-(hydroxymethyl)acetamide
tert-butyl 3,5-dihydroxy-6-mercapto-3-methylhexanoate
6-<<(acetamidomethyl)thio>methyl>-4-hydroxy-4-methyl-3,4,5,6-tetrahydro-2H-pyran-2-one
Conditions | Yield |
---|---|
With formic acid for 2h; Ambient temperature; | 69.2% |
N-(hydroxymethyl)acetamide
6-benzylthio-2-phenylimidazo<1,2-b>pyridazine
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid for 14h; Heating; | 66% |
formaldehyd
1-methyl-4-nitrobenzene
N-(hydroxymethyl)acetamide
A
bis-(2-methyl-5-nitro-phenyl)-methane
B
N-(2-methyl-5-nitrobenzyl)acetamide
Conditions | Yield |
---|---|
In sulfuric acid at 55℃; for 8h; | A n/a B 65% |
N-(hydroxymethyl)acetamide
6-fluoro-2-phenylimidazo<1,2-b>pyridazine
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid for 14h; Heating; | 65% |
N-(hydroxymethyl)acetamide
thioacetic acid
S-(acetylamino)methyl thioacetate
Conditions | Yield |
---|---|
64% |
N-(hydroxymethyl)acetamide
potassium thioacetate
S-(acetylamino)methyl thioacetate
Conditions | Yield |
---|---|
With potassium carbonate at 40℃; for 70h; Inert atmosphere; | 64% |
Conditions | Yield |
---|---|
With sulfuric acid at 0 - 20℃; for 12h; | 64% |
N-(hydroxymethyl)acetamide
3-mercaptopropionic acid
3-{[(acetylamino)methyl]sulfanyl}-propionic acid
Conditions | Yield |
---|---|
In trifluoroacetic acid for 0.5h; Ambient temperature; | 62% |
Conditions | Yield |
---|---|
With sulfuric acid In acetic acid for 14h; Heating; | 62% |
N-(hydroxymethyl)acetamide
2-(4-tert-Butyl-phenyl)-6-phenylsulfanyl-imidazo[1,2-b]pyridazine
Conditions | Yield |
---|---|
With sulfuric acid at 100℃; for 14h; | 56% |
With sulfuric acid In acetic acid for 14h; Heating; | 56% |
Conditions | Yield |
---|---|
Stage #1: C23H24ClNS With chlorotriisopropylsilane; trifluorormethanesulfonic acid; trifluoroacetic acid at 0℃; for 0.5h; Stage #2: N-(hydroxymethyl)acetamide at 0 - 20℃; for 2.5h; | 55% |
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