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inquiryUnique advantages Guaranteed purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White or light yellow crystalline powder Storage:cool dry place Package:1g/foil bag Application:pharmaceutical int
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inquiryProduct Name: 3,5-Dimethyl-4-hydroxybenzaldehyde CAS: 2233-18-3 MF: C9H10O2 MW: 150.17 EINECS: 218-774-5 Mol File: 2233-18-3.mol 3,5-Dimethyl-4-hydroxybenzaldehyde Structure 3,5-Dimethyl-4-hydroxybenzaldehyde Chemical Properties M
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inquiryProduct name: 3,5-Dimethyl-4-Hydroxybenzaldehyde CAS No.: 2233-18-3 Molecule Formula:C9H10O2 Molecule Weight:150.17 Purity: 99.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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inquiry4-hydroxy-2,4,6-trimethyl-cyclohexa-2,5-dienone
B
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With sodium hypochlorite In water; ethyl acetate | A n/a B 100% |
Conditions | Yield |
---|---|
With copper diacetate; ethylene glycol at 50℃; for 8h; Green chemistry; regioselective reaction; | 92% |
With ammonium acetate; potassium hexacyanoferrate(III) In methanol; water at 45℃; for 10h; | 90% |
With dimethyl selenoxide In benzene for 1.5h; Heating; | 80% |
2.6-dimethylphenol
hexamethylenetetramine
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
In trifluoroacetic acid at 80℃; for 12h; Duff reaction; | 92% |
With acetic acid In water for 4h; Reflux; Inert atmosphere; | 70% |
With acetic acid In water at 100℃; for 4h; | |
With acetic acid In water at 105 - 120℃; for 6h; Duff Aldehyde Synthesis; Dean-Stark; |
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With oxygen; cobalt(II) acetate; sodium hydroxide In water; ethylene glycol at 50℃; under 760.051 Torr; for 12h; Green chemistry; | 90% |
Conditions | Yield |
---|---|
With oxygen; cobalt(II) acetate; sodium hydroxide In water; ethylene glycol at 50℃; under 760.051 Torr; for 12h; Reagent/catalyst; Solvent; Time; Green chemistry; chemoselective reaction; | 88% |
With copper diacetate; ethylene glycol at 65℃; for 12h; Green chemistry; regioselective reaction; | 87% |
With 2.9-dimethyl-1,10-phenanthroline; sodium methylate In methanol for 0.75h; | 85% |
Mesitol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-1,4-benzoquinone
Conditions | Yield |
---|---|
With oxygen; acetone oxime In various solvent(s) at 40℃; under 860.3 Torr; for 6h; | A 87% B 4% |
With oxygen In various solvent(s) at 60℃; under 860.3 Torr; for 5h; Product distribution; Mechanism; Rate constant; var. aditives, times, solvents; | A 77.7% B 3.7% |
With oxygen; diethylamine In various solvent(s) at 60℃; under 860.3 Torr; for 4h; Product distribution; other amines; variation of condition; | |
With oxygen; diethylamine In various solvent(s) at 60℃; under 860.3 Torr; for 4h; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With copper diacetate; ethylene glycol at 50℃; for 8h; Green chemistry; regioselective reaction; | 85% |
With ammonium acetate; potassium hexacyanoferrate(III) In methanol; water at 45℃; for 240h; | 82% |
Multi-step reaction with 2 steps 1: 20 °C 2: 280 mg / H2O / 20 °C View Scheme |
methanol
Mesitol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-4-(methoxymethyl)phenol
Conditions | Yield |
---|---|
With potassium hydroxide; iodine for 0.166667h; | A 5% B 84% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 6h; Mechanism; other alcohols, var. times; | A 4% B 64% |
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 6h; | A 4% B 64% |
Mesitol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
4-(hydroxymethyl)-2,6-dimethylphenol
Conditions | Yield |
---|---|
With oxygen; horseradish peroxidase pH=7; Oxidation; electrolysis after 3 F; | A n/a B 83% |
With iron(III) perchlorate In water Kinetics; |
4-(1,3-diphenyl-imidazolidin-2-yl)-2,6-dimethyl-phenol
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With hydrogenchloride; water at 25℃; for 2h; | 80% |
2.6-dimethylphenol
Dichloromethyl methyl ether
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
Stage #1: 2.6-dimethylphenol With aluminum (III) chloride In dichloromethane at 20℃; for 0.166667h; Inert atmosphere; Stage #2: Dichloromethyl methyl ether In dichloromethane at 20℃; for 0.166667h; Inert atmosphere; | 71% |
Stage #1: 2.6-dimethylphenol With aluminum (III) chloride In dichloromethane at 0℃; for 0.166667h; Inert atmosphere; Stage #2: Dichloromethyl methyl ether In dichloromethane for 0.5h; Inert atmosphere; |
4-(hydroxymethyl)-2,6-dimethylphenol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-1,4-benzoquinone
Conditions | Yield |
---|---|
With oxygen; amine>cobalt In dichloromethane under 2585.7 Torr; for 20h; Ambient temperature; | A n/a B 70% |
With K10 montmorillonite; water; dihydrogen peroxide In tetrachloromethane at 22℃; for 2h; Oxidation; | A 3 % Chromat. B 57 % Chromat. |
Mesitol
water
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-4-(methoxymethyl)phenol
Conditions | Yield |
---|---|
platinum In methanol | A 70% B n/a |
Conditions | Yield |
---|---|
With hexamethylenetetramine In trifluoroacetic acid at 80℃; for 20h; Inert atmosphere; | 67% |
Multi-step reaction with 2 steps 1: 76 percent / H2O / 2.5 h / 30 °C 2: 64 percent / pyridinium chlorochromate, sodium acetate / CH2Cl2 / 2 h View Scheme | |
Multi-step reaction with 2 steps 1: aqueous NaOH 2: 230 - 240 °C View Scheme |
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With tin(ll) chloride In 1,4-dioxane Heating; | 63% |
Mesitol
hexan-1-ol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-4-(hexyloxymethyl)phenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 1.11667h; | A 14% B 63% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 1.11667h; Yield given. Yields of byproduct given; |
pentan-1-ol
Mesitol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-4-(pentyloxymethyl)phenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 1.13333h; | A 24% B 61% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 1.13333h; Yield given. Yields of byproduct given; |
propan-1-ol
Mesitol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-4-(propoxymethyl)phenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 1.08333h; | A 6% B 60% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 1.08333h; Yield given. Yields of byproduct given; |
ethanol
Mesitol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
4-(ethoxymethyl)-2,6-dimethylphenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 1.65h; | A 4% B 59% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 1.65h; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With oxygen; cobalt(II) acetate; sodium hydroxide In water at 50℃; under 760.051 Torr; for 3h; Mechanism; Green chemistry; regioselective reaction; | A 30% B 58% |
Mesitol
butan-1-ol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
4-(butoxymethyl)-2,6-dimethylphenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 1.08333h; | A 6% B 55% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 1.08333h; Yield given. Yields of byproduct given; |
Mesitol
cyclohexanol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
4-(cyclohexyloxymethyl)-2,6-dimethylphenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 5h; | A 10% B 51% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 5h; Yield given. Yields of byproduct given; |
3,5-dimethyl-4-hydroxybenzyl bromide
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With dipotassium hydrogenphosphate; dimethyl selenoxide In 1,2-dichloro-ethane for 0.5h; Heating; | 49% |
(E)-2,6-dimethyl-4-styrylphenol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
benzaldehyde
Conditions | Yield |
---|---|
With oxygen; CoSMDPT In 1,2-dichloro-ethane at 25℃; for 5h; | A 48% B 46% |
Mesitol
isopropyl alcohol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
2,6-dimethyl-4-(isopropoxymethyl)phenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 0.733333h; | A 21% B 45% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 0.733333h; Yield given. Yields of byproduct given; |
Mesitol
tert-butyl alcohol
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
4-(t-butoxymethyl)-2,6-dimethylphenol
Conditions | Yield |
---|---|
With oxygen; copper dichloride; acetone oxime at 40℃; under 860.3 Torr; for 7h; | A 10% B 12% |
With oxygen; acetone oxime at 40℃; under 860.3 Torr; for 7h; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With hydrogenchloride; aluminium trichloride; benzene zunaechst unter Kuehlung, schliesslich bei 40grad; man giesst das Reaktionsgemisch auf Eis, saeuert mit Salzsaeure an und destilliert mit Wasserdampf; |
4-(hydroxymethyl)-2,6-dimethylphenol
A
Mesitol
B
4-hydroxy-3,5-dimethylbenzaldehyde
C
3,5,3',5'-tetramethyl-stilbene-4,4'-diol
D
4,4’-(ethane-1,2-diyl)bis(2,6-dimethylphenol)
Conditions | Yield |
---|---|
at 230 - 240℃; |
4,4'-(oxybis(methylene))bis(2,6-dimethylphenol)
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
at 200℃; |
4,4'-(oxybis(methylene))bis(2,6-dimethylphenol)
A
4-hydroxy-3,5-dimethylbenzaldehyde
B
3,5,3',5'-tetramethyl-stilbene-4,4'-diol
C
4,4’-(ethane-1,2-diyl)bis(2,6-dimethylphenol)
Conditions | Yield |
---|---|
at 200℃; |
4-hydroxy-3,5-dimethylbenzaldehyde
chloromethyl methyl ether
4-(methoxymethoxy)-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
Stage #1: 4-hydroxy-3,5-dimethylbenzaldehyde With potassium carbonate In acetone at 20℃; for 0.25h; Stage #2: chloromethyl methyl ether In acetone for 2h; Reflux; | 100% |
Stage #1: 4-hydroxy-3,5-dimethylbenzaldehyde With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere; Stage #2: chloromethyl methyl ether In N,N-dimethyl-formamide at 0 - 20℃; for 16h; Inert atmosphere; | 92% |
Stage #1: 4-hydroxy-3,5-dimethylbenzaldehyde With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 1h; Inert atmosphere; Stage #2: chloromethyl methyl ether In N,N-dimethyl-formamide at 20℃; for 16h; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
With sodium acetate In water at 80℃; for 2h; | 100% |
4-hydroxy-3,5-dimethylbenzaldehyde
3,5-dimethyl-4-(3'-iso-propyl-4'-methoxyphenoxy)benzaldehyde
Conditions | Yield |
---|---|
With copper; triethylamine In dichloromethane at 0 - 20℃; for 72h; | 100% |
With copper; triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
With copper; triethylamine In dichloromethane at 0 - 20℃; for 72h; | 100% |
With copper bronze; triethylamine In dichloromethane at 0 - 20℃; for 16h; | 93% |
4-hydroxy-3,5-dimethylbenzaldehyde
4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile
Conditions | Yield |
---|---|
With 1-methyl-pyrrolidin-2-one; sodium hydride In 1,4-dioxane at 150℃; for 12h; | 100% |
With sodium hydride In 1,4-dioxane; 1-methyl-pyrrolidin-2-one for 18.33h; Heating / reflux; | 98% |
o-fluorobenzyl bromide
4-hydroxy-3,5-dimethylbenzaldehyde
4-(2-Fluoro-benzyloxy)-3,5-dimethyl-benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In DMF (N,N-dimethyl-formamide) at 90℃; | 100% |
With potassium carbonate; potassium iodide In DMF (N,N-dimethyl-formamide) |
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 90℃; | 100% |
bromethyl methyl ether
4-hydroxy-3,5-dimethylbenzaldehyde
4-(methoxymethoxy)-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at 0℃; for 0.5h; | 100% |
4-hydroxy-3,5-dimethylbenzaldehyde
5-bromoanthranilamide
6-bromo-2-(4-hydroxy-3,5-dimethylphenyl)quinazolin-4(3H)-one
Conditions | Yield |
---|---|
With iodine In ethanol for 4h; Inert atmosphere; Reflux; | 100% |
With toluene-4-sulfonic acid; sodium hydrogensulfite In N,N-dimethyl acetamide at 135℃; for 2.5h; | 68% |
With sodium hydrogen sulfate; toluene-4-sulfonic acid In N,N-dimethyl acetamide at 135℃; for 2.5h; | 68% |
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With sulfuric acid In 1,4-dioxane at 20℃; for 72h; | 100% |
4-hydroxy-3,5-dimethylbenzaldehyde
anthranilic acid amide
Conditions | Yield |
---|---|
With iodine In ethanol for 4h; Inert atmosphere; Reflux; | 100% |
4-hydroxy-3,5-dimethylbenzaldehyde
2-amino-6-fluorobenzamide
Conditions | Yield |
---|---|
With iodine In ethanol for 4h; Inert atmosphere; Reflux; | 100% |
4-hydroxy-3,5-dimethylbenzaldehyde
2-amino-5-fluorobenzamide
Conditions | Yield |
---|---|
With iodine In ethanol for 4h; Inert atmosphere; Reflux; | 100% |
Conditions | Yield |
---|---|
With iodine In ethanol for 4h; Inert atmosphere; Reflux; | 100% |
Conditions | Yield |
---|---|
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 2h; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 2h; | 100% |
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 2h; |
4-hydroxy-3,5-dimethylbenzaldehyde
1-iodo-propane
3,5-dimethyl-4-(propyloxy)benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 80℃; for 20h; Inert atmosphere; | 99% |
With potassium carbonate In acetonitrile for 18h; Heating; | 96% |
4-hydroxy-3,5-dimethylbenzaldehyde
benzyl bromide
3,5-dimethyl-4-benzyloxy benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; for 16h; Heating / reflux; | 99% |
With potassium carbonate In acetone at 50℃; for 2.5h; | 99% |
Stage #1: 4-hydroxy-3,5-dimethylbenzaldehyde With sodium hydride In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: benzyl bromide In N,N-dimethyl-formamide at 20℃; for 16h; Stage #3: With acetic acid In water; N,N-dimethyl-formamide pH=4 - 5; | 95% |
trifluoromethylsulfonic anhydride
4-hydroxy-3,5-dimethylbenzaldehyde
trifluoromethanesulfonic acid 4-formyl-2,6-dimethoxyphenyl ester
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 20℃; for 16h; | 98.9% |
4-hydroxy-3,5-dimethylbenzaldehyde
4-chloro-2-[2-(hydrazinecarbonyl)phenylamino]benzohydrazide
4-chloro-N'-(4-hydroxy-3,5-dimethylbenzylidene)-2-{2-[2(4-hydroxy-3,5-dimethylbenzylidene)hydrazinecarbonyl]phenylamino}benzohydrazide
Conditions | Yield |
---|---|
With acetic acid In ethanol Reflux; | 98.5% |
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With ammonium acetate In methanol at 20℃; | 98% |
4-chloro-6-nitroquinoline
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 120℃; for 5h; Sealed tube; | 97% |
4-hydroxy-3,5-dimethylbenzaldehyde
methyl iodide
3,5-dimethyl-4-methoxybenzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 20℃; for 12h; | 96% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 18h; | 95% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 18h; | 95% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 18h; | 61% |
With potassium carbonate In acetone for 96h; Inert atmosphere; Reflux; |
[1,3]-dioxolan-2-one
4-hydroxy-3,5-dimethylbenzaldehyde
4-(2-hydroxy ethoxy)-3,5-dimethyl benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 110℃; | 96% |
With potassium carbonate In N,N-dimethyl-formamide at 110℃; Inert atmosphere; | 78.8% |
4-hydroxy-3,5-dimethylbenzaldehyde
2-chloro-ethanol
4-(2-hydroxy ethoxy)-3,5-dimethyl benzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In ethanol for 24h; Heating / reflux; | 95% |
With potassium carbonate In ethanol for 24h; Reflux; | 95% |
With potassium carbonate In ethanol for 24h; | 95% |
2,4-dichlorothieno[3,2-d]pyrimidine
4-hydroxy-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
Stage #1: 4-hydroxy-3,5-dimethylbenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: 2,4-dichlorothieno[3,2-d]pyrimidine In N,N-dimethyl-formamide at 20℃; for 1h; | 95% |
Stage #1: 4-hydroxy-3,5-dimethylbenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 0.25h; Stage #2: 2,4-dichlorothieno[3,2-d]pyrimidine In N,N-dimethyl-formamide at 20℃; for 1h; | 95% |
Stage #1: 2,4-dichlorothieno[3,2-d]pyrimidine With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.25h; Stage #2: 4-hydroxy-3,5-dimethylbenzaldehyde In N,N-dimethyl-formamide for 1.5h; | 91.3% |
Stage #1: 4-hydroxy-3,5-dimethylbenzaldehyde With potassium carbonate In N,N-dimethyl-formamide at 25℃; for 0.25h; Stage #2: 2,4-dichlorothieno[3,2-d]pyrimidine In N,N-dimethyl-formamide at 25℃; for 1.5h; | 90% |
4-hydroxy-3,5-dimethylbenzaldehyde
2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 100℃; for 12h; | 94.9% |
With potassium carbonate In N,N-dimethyl-formamide | |
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 100℃; for 12h; | |
With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 100℃; for 12h; |
4-hydroxy-3,5-dimethylbenzaldehyde
2-nitrophenylmethyl bromide
4-(2'-nitrobenzyloxy)-3,5-dimethylbenzaldehyde
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 3.5h; Etherification; alkylation; | 94% |
With potassium carbonate In DMF (N,N-dimethyl-formamide) at 20℃; for 2h; | 88% |
With potassium hydride In DMF (N,N-dimethyl-formamide) at -23℃; |
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In ethyl acetate at 70℃; for 5h; | 94% |
4-hydroxy-3,5-dimethylbenzaldehyde
5,6-dimethoxybenzo[b]thiophen-3(2H)-one
Conditions | Yield |
---|---|
With piperidine In toluene at 80℃; for 2h; Schlenk technique; Molecular sieve; Inert atmosphere; | 94% |
4-hydroxy-3,5-dimethylbenzaldehyde
2-amino-4-bromobenzamide
Conditions | Yield |
---|---|
With iodine In ethanol for 4h; Inert atmosphere; Reflux; | 94% |
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