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inquiry3,4-(Methylenedioxy)cinnamic acid CAS:2373-80-0 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality
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inquiry3,4-(Methylenedioxy)cinnamic acidAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air
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inquiry3,4-(Methylenedioxy)cinnamic acid cas 2373-80-0Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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inquirygood quality, competitive price, thoughtful after sale serviceAppearance:white powder Storage:Keep it in dry,shady and cool place Package:5g Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by express or by sea Port:Any port
methyl (2E)-3-(1,3-benzodioxol-5-yl)acrylate
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Stage #1: methyl (2E)-3-(1,3-benzodioxol-5-yl)acrylate With water; sodium hydroxide In tetrahydrofuran Stage #2: With hydrogenchloride In water pH=< 3; | 99% |
With sodium hydroxide In tetrahydrofuran; methanol at 40℃; Inert atmosphere; | 81% |
With potassium hydroxide In ethanol; water Heating; | 15 mg |
Conditions | Yield |
---|---|
With aluminum oxide; lithium chloride for 0.1h; Doebner condensation; microwave irradiation; | 98% |
With piperidine; pyridine for 1h; Knoevenagel-Doebner-Stobbe Reaction; Reflux; | 98% |
With ammonium acetate for 0.0666667h; Irradiation; | 97% |
Conditions | Yield |
---|---|
Stage #1: piperonal; acetic acid With titanium tetrachloride In dichloromethane at 25℃; for 0.333333h; Inert atmosphere; Stage #2: With triethylamine In dichloromethane at 25℃; Inert atmosphere; stereoselective reaction; | 98% |
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With zinc In acetic acid at 20℃; for 0.0166667h; microwave irradiation; | 96% |
3,4-methylenedioxycinnamic acid benzhydryl ester
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With formic acid at 40 - 45℃; for 0.5h; Product distribution; | 89% |
(E)-2'-hydroxy-3,4-methylenedioxychalcone
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide; potassium carbonate In acetonitrile at 20℃; for 5h; | 89% |
piperonal
malonic acid
A
5-vinyl-1,3-benzodioxole
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With pyridine; acetic acid at 130℃; for 0.133333h; Knoevenagel-Doebner reaction; microwave irradiation; | A 4 % Spectr. B 85% |
Conditions | Yield |
---|---|
With potassium acetate for 6h; Heating; | 50% |
With sodium acetate |
wikstromol
A
4-Benzenesulfonylamino-2-benzo[1,3]dioxol-5-ylmethyl-4-oxo-3-(3,4,5-trimethoxy-benzyl)-butyric acid
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With n-butyllithium 1) -78 --> 0 deg C, several hours; 2) -78 --> RT; Yield given. Multistep reaction; | A n/a B 30% |
piperonal
sodium acetate
acetic anhydride
3,4-methylenedioxy-trans-cinnamic acid
piperonal
malonic acid
acetic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With sodium Behandeln mit methylalkoholischer Kalilauge; |
piperonal
malonic acid
dimethyl amine
B
3,4-methylenedioxy-trans-cinnamic acid
ethyl (E)-3-(benzo[d][1,3]dioxol-5-yl)acrylate
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With potassium hydroxide | |
With water; potassium hydroxide In tetrahydrofuran |
3-(3,4,5-trimethoxyphenyl)propanoic acid
A
2-piperonyl-3-(3,4,5-trimethoxy-benzyl)-succinic acid
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With lithium diisopropyl amide Yield given; |
piperonal
malonic acid
ammonia
3,4-methylenedioxy-trans-cinnamic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With potassium hydroxide |
ethanol
dihydrogen peroxide
4-benzo[1,3]dioxol-5-yl-2-oxo-but-3-enoic acid
3,4-methylenedioxy-trans-cinnamic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With ethanol; dihydrogen peroxide |
piperonal
malonic acid
ammonia
A
piperonylidene-malonic acid
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 304 mg / conc. H2SO4 / 1 h / Heating 2: K2CO3, Cu0 / dimethylformamide / 1 h / Heating 3: 15 mg / KOH / ethanol; H2O / Heating View Scheme |
Methyl caffeate
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: K2CO3, Cu0 / dimethylformamide / 1 h / Heating 2: 15 mg / KOH / ethanol; H2O / Heating View Scheme | |
Multi-step reaction with 2 steps 1: potassium carbonate / N,N-dimethyl-formamide / 110 °C / Inert atmosphere 2: sodium hydroxide / methanol; tetrahydrofuran / 40 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 1.) LDA, 2.) CBr4 / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 2 h 2: 92 percent / KI / acetone / 24 h / Heating 3: NaH / 0 °C 4: 1.) LDA View Scheme | |
Multi-step reaction with 4 steps 1: 1.) LDA, 2.) CBr4 / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 2 h 2: 92 percent / KI / acetone / 24 h / Heating 3: NaH / 0 °C 4: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme | |
Multi-step reaction with 3 steps 1: 1.) LDA, 2.) iodine / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 10 min 2: NaH / 0 °C 3: 1.) LDA View Scheme | |
Multi-step reaction with 3 steps 1: 1.) LDA, 2.) iodine / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 10 min 2: NaH / 0 °C 3: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme |
3-(3,4-methylenedioxyphenyl)-2-bromopropionic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 92 percent / KI / acetone / 24 h / Heating 2: NaH / 0 °C 3: 1.) LDA View Scheme | |
Multi-step reaction with 3 steps 1: 92 percent / KI / acetone / 24 h / Heating 2: NaH / 0 °C 3: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme |
3-Benzo[1,3]dioxol-5-yl-2-iodo-propionic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaH / 0 °C 2: 1.) LDA View Scheme | |
Multi-step reaction with 2 steps 1: NaH / 0 °C 2: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pyridine; piperidine 2: ethanolic KOH-solution View Scheme | |
Multi-step reaction with 2 steps 1: sodium hydride / tetrahydrofuran / 0 °C 2: potassium hydroxide; water / tetrahydrofuran View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: potassium carbonate / 60 °C 2: pyridine; piperidine / 24 h / 80 °C View Scheme | |
Multi-step reaction with 2 steps 1: potassium carbonate / acetone / 29 h / 50 - 60 °C 2: pyridine; piperidine / 24 h / 80 - 90 °C View Scheme | |
Multi-step reaction with 2 steps 1.1: caesium carbonate / N,N-dimethyl-formamide / 24 h / 100 °C 2.1: pyridine / 0.17 h / 20 °C 2.2: 4 h / Reflux View Scheme | |
Multi-step reaction with 2 steps 1: potassium carbonate / Reflux 2: pyridine; piperidine / 24 h / 80 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 12 h / 80 °C 2: acetic anhydride / isopropyl alcohol / 1 h / 55 - 110 °C 3: piperidine; pyridine / 2 h / 115 °C View Scheme | |
Multi-step reaction with 3 steps 1.1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 12 h / 80 °C 2.1: acetic anhydride / isopropyl alcohol / 0.5 h / 55 °C 2.2: 1 h / 110 °C 2.3: 3 h 3.1: pyridine; piperidine / 2 h / 115 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: acetic anhydride / isopropyl alcohol / 1 h / 55 - 110 °C 2: piperidine; pyridine / 2 h / 115 °C View Scheme | |
Multi-step reaction with 2 steps 1.1: acetic anhydride / isopropyl alcohol / 0.5 h / 55 °C 1.2: 1 h / 110 °C 1.3: 3 h 2.1: pyridine; piperidine / 2 h / 115 °C View Scheme |
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In N,N-dimethyl-formamide under 760 Torr; for 24h; | 100% |
With palladium 10% on activated carbon; hydrogen; acetic acid In methanol at 20℃; for 22h; | 99% |
With 10% Pd/C; cyclohexa-1,4-diene In methanol at 100℃; for 0.0833333h; Microwave irradiation; | 95% |
3,4-methylenedioxy-trans-cinnamic acid
(E)-3-(1,3-benzodioxol-5-yl)acryloyl chloride
Conditions | Yield |
---|---|
With oxalyl dichloride at 25℃; for 0.5h; | 100% |
With oxalyl dichloride at 25℃; for 2h; | 100% |
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 0 - 20℃; | 100% |
methanol
3,4-methylenedioxy-trans-cinnamic acid
methyl (2E)-3-(1,3-benzodioxol-5-yl)acrylate
Conditions | Yield |
---|---|
With sulfuric acid Heating; | 99% |
With sulfuric acid for 24h; Reflux; | 98% |
With sulfuric acid for 0.166667h; Esterification; Irradiation; | 96% |
diazomethane
3,4-methylenedioxy-trans-cinnamic acid
methyl (2E)-3-(1,3-benzodioxol-5-yl)acrylate
Conditions | Yield |
---|---|
In methanol; diethyl ether at 20℃; for 0.25h; Inert atmosphere; | 99% |
2 g | |
In methanol; diethyl ether at 0℃; for 0.666667h; Esterification; |
4-Chloro-3,5-dimethylphenol
3,4-methylenedioxy-trans-cinnamic acid
4-(benzo[d][1,3]dioxol-5-yl)-6-chloro-5,7-dimethyl-3,4-dihydrochromen-2-one
Conditions | Yield |
---|---|
With trifluoroacetic acid for 23h; | 99% |
With trifluoroacetic acid |
methyl (2E)-3-(1,3-benzodioxol-5-yl)acrylate
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Stage #1: methyl (2E)-3-(1,3-benzodioxol-5-yl)acrylate With water; sodium hydroxide In tetrahydrofuran Stage #2: With hydrogenchloride In water pH=< 3; | 99% |
With sodium hydroxide In tetrahydrofuran; methanol at 40℃; Inert atmosphere; | 81% |
With potassium hydroxide In ethanol; water Heating; | 15 mg |
Conditions | Yield |
---|---|
With aluminum oxide; lithium chloride for 0.1h; Doebner condensation; microwave irradiation; | 98% |
With piperidine; pyridine for 1h; Knoevenagel-Doebner-Stobbe Reaction; Reflux; | 98% |
With ammonium acetate for 0.0666667h; Irradiation; | 97% |
Conditions | Yield |
---|---|
Stage #1: piperonal; acetic acid With titanium tetrachloride In dichloromethane at 25℃; for 0.333333h; Inert atmosphere; Stage #2: With triethylamine In dichloromethane at 25℃; Inert atmosphere; stereoselective reaction; | 98% |
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With zinc In acetic acid at 20℃; for 0.0166667h; microwave irradiation; | 96% |
3,4-methylenedioxycinnamic acid benzhydryl ester
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With formic acid at 40 - 45℃; for 0.5h; Product distribution; | 89% |
(E)-2'-hydroxy-3,4-methylenedioxychalcone
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With dihydrogen peroxide; potassium carbonate In acetonitrile at 20℃; for 5h; | 89% |
piperonal
malonic acid
A
5-vinyl-1,3-benzodioxole
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With pyridine; acetic acid at 130℃; for 0.133333h; Knoevenagel-Doebner reaction; microwave irradiation; | A 4 % Spectr. B 85% |
Conditions | Yield |
---|---|
With potassium acetate for 6h; Heating; | 50% |
With sodium acetate |
wikstromol
A
4-Benzenesulfonylamino-2-benzo[1,3]dioxol-5-ylmethyl-4-oxo-3-(3,4,5-trimethoxy-benzyl)-butyric acid
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With n-butyllithium 1) -78 --> 0 deg C, several hours; 2) -78 --> RT; Yield given. Multistep reaction; | A n/a B 30% |
piperonal
sodium acetate
acetic anhydride
3,4-methylenedioxy-trans-cinnamic acid
piperonal
malonic acid
acetic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With sodium Behandeln mit methylalkoholischer Kalilauge; |
piperonal
malonic acid
dimethyl amine
B
3,4-methylenedioxy-trans-cinnamic acid
ethyl (E)-3-(benzo[d][1,3]dioxol-5-yl)acrylate
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With potassium hydroxide | |
With water; potassium hydroxide In tetrahydrofuran |
3-(3,4,5-trimethoxyphenyl)propanoic acid
A
2-piperonyl-3-(3,4,5-trimethoxy-benzyl)-succinic acid
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With lithium diisopropyl amide Yield given; |
piperonal
malonic acid
ammonia
3,4-methylenedioxy-trans-cinnamic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With potassium hydroxide |
ethanol
dihydrogen peroxide
4-benzo[1,3]dioxol-5-yl-2-oxo-but-3-enoic acid
3,4-methylenedioxy-trans-cinnamic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
With ethanol; dihydrogen peroxide |
piperonal
malonic acid
ammonia
A
piperonylidene-malonic acid
B
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 304 mg / conc. H2SO4 / 1 h / Heating 2: K2CO3, Cu0 / dimethylformamide / 1 h / Heating 3: 15 mg / KOH / ethanol; H2O / Heating View Scheme |
Methyl caffeate
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: K2CO3, Cu0 / dimethylformamide / 1 h / Heating 2: 15 mg / KOH / ethanol; H2O / Heating View Scheme | |
Multi-step reaction with 2 steps 1: potassium carbonate / N,N-dimethyl-formamide / 110 °C / Inert atmosphere 2: sodium hydroxide / methanol; tetrahydrofuran / 40 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 1.) LDA, 2.) CBr4 / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 2 h 2: 92 percent / KI / acetone / 24 h / Heating 3: NaH / 0 °C 4: 1.) LDA View Scheme | |
Multi-step reaction with 4 steps 1: 1.) LDA, 2.) CBr4 / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 2 h 2: 92 percent / KI / acetone / 24 h / Heating 3: NaH / 0 °C 4: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme | |
Multi-step reaction with 3 steps 1: 1.) LDA, 2.) iodine / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 10 min 2: NaH / 0 °C 3: 1.) LDA View Scheme | |
Multi-step reaction with 3 steps 1: 1.) LDA, 2.) iodine / 1) THF, -78 deg C (45 min), 0 deg C (3 1/4 h), RT (1 h); 2) THF, -78 deg C, 10 min 2: NaH / 0 °C 3: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme |
3-(3,4-methylenedioxyphenyl)-2-bromopropionic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 92 percent / KI / acetone / 24 h / Heating 2: NaH / 0 °C 3: 1.) LDA View Scheme | |
Multi-step reaction with 3 steps 1: 92 percent / KI / acetone / 24 h / Heating 2: NaH / 0 °C 3: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme |
3-Benzo[1,3]dioxol-5-yl-2-iodo-propionic acid
3,4-methylenedioxy-trans-cinnamic acid
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaH / 0 °C 2: 1.) LDA View Scheme | |
Multi-step reaction with 2 steps 1: NaH / 0 °C 2: 30 percent / 1.) n-BuLi / 1) -78 --> 0 deg C, several hours; 2) -78 --> RT View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pyridine; piperidine 2: ethanolic KOH-solution View Scheme | |
Multi-step reaction with 2 steps 1: sodium hydride / tetrahydrofuran / 0 °C 2: potassium hydroxide; water / tetrahydrofuran View Scheme |
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