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4-allylpyrocatechol
Conditions | Yield |
---|---|
With water | 100% |
Conditions | Yield |
---|---|
With pyridine; aluminium(III) iodide In acetonitrile at 80℃; for 18h; Reagent/catalyst; Solvent; | 99% |
Stage #1: 4-allylguaiacol With pyridine; iodine; aluminium In acetonitrile for 18h; Reflux; Stage #2: With hydrogenchloride In water; acetonitrile at 20℃; Reagent/catalyst; | 99% |
With aluminium(III) iodide; diisopropyl-carbodiimide In acetonitrile at 80℃; for 18h; Reagent/catalyst; | 99% |
Conditions | Yield |
---|---|
With aluminium(III) iodide; diisopropyl-carbodiimide In acetonitrile at 80℃; for 18h; | 99% |
With aluminium(III) iodide In dimethyl sulfoxide; acetonitrile at 80℃; for 18h; | 96% |
With aluminium(III) iodide; dimethyl sulfoxide In acetonitrile at 80℃; for 18h; | 96% |
Conditions | Yield |
---|---|
With boron trichloride; tetra-(n-butyl)ammonium iodide In dichloromethane at -78℃; for 1h; dealkylation; | 88% |
With boron trifluoride diethyl etherate In 1,4-dioxane at 20℃; for 24h; Inert atmosphere; | 55.1% |
With boron tribromide In dichloromethane at -78 - 0℃; for 1h; | 27% |
((4-allyl-1,2-phenylene)bis(oxy))bis(triethylsilane)
4-allylpyrocatechol
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran; water Inert atmosphere; | 70% |
With hydrogenchloride In tetrahydrofuran; water at 20℃; Inert atmosphere; | 54% |
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In dichloromethane at -78℃; | 62% |
2-allyloxyphenol
A
4-allylpyrocatechol
B
3-(2-propenyl)-1,2-benzenediol
Conditions | Yield |
---|---|
at 170℃; Inert atmosphere; Neat (no solvent); | A 18% B 54% |
at 170℃; for 2h; Inert atmosphere; | A 18% B 54% |
In neat (no solvent) at 170℃; for 3h; Claisen Rearrangement; Inert atmosphere; Sealed tube; | A 27% B 40% |
Conditions | Yield |
---|---|
With sodium carbonate; copper(l) chloride In water at 20℃; for 0.5h; | 54% |
Conditions | Yield |
---|---|
With caesium carbonate In 2,2,2-trifluoroethanol for 24h; Irradiation; | 47% |
Conditions | Yield |
---|---|
With aluminium(III) iodide; N,N-dimethyl-formamide dimethyl acetal In acetonitrile at 80℃; for 18h; | 27% |
With aluminium(III) iodide; N,N-dimethyl-formamide dimethyl acetal In acetonitrile at 80℃; for 18h; | 27% |
methyl magnesium iodide
1,2-dimethoxy-4-(2-propenyl)benzene
4-allylpyrocatechol
Conditions | Yield |
---|---|
With diethyl ether; xylene at 175 - 180℃; Erhitzen des vom Aether befreiten Reaktionsgemisches unter Stickstoff; |
tetrachloromethane
diethyl ether
1,2-dimethoxy-4-(2-propenyl)benzene
4-allylpyrocatechol
Conditions | Yield |
---|---|
Erhitzen des vom Aether befreiten Reaktionsgemisches auf 160-180grad; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: Larrea tridentata cinnamyl alcohol acyltransferase-1 / aq. buffer / 0.5 h / 30 °C / pH 7.9 / Enzymatic reaction 2: NADH; propenylphenol synthase from Larrea tridentata / aq. buffer / 30 °C / pH 6.5 View Scheme |
4-allylpyrocatechol
Conditions | Yield |
---|---|
With propenylphenol synthase from Larrea tridentata; NADH In aq. buffer at 30℃; pH=6.5; Kinetics; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: potassium carbonate / acetone / 1 h / 20 °C 1.2: 5.5 h / 20 - 70 °C 2.1: 2 h / 170 °C / Inert atmosphere View Scheme |
Conditions | Yield |
---|---|
With aluminium(III) iodide; dimethyl sulfoxide In acetonitrile at 80℃; for 18h; Reagent/catalyst; | |
With aluminium(III) iodide; N,N-dimethyl-formamide In acetonitrile at 80℃; for 18h; Reagent/catalyst; |
benzene-1,2-diol
A
4-allylpyrocatechol
B
3-(2-propenyl)-1,2-benzenediol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: potassium carbonate / acetone / 0.5 h / 20 °C 1.2: 3.5 h / Reflux 2.1: neat (no solvent) / 3 h / 170 °C / Inert atmosphere; Sealed tube View Scheme |
Conditions | Yield |
---|---|
With tris(pentafluorophenyl)borate |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; for 1h; Inert atmosphere; | 100% |
With hydrogen; palladium 10% on activated carbon In methanol at 20℃; for 2h; | 95% |
With methanol; palladium 10% on activated carbon at 20℃; for 2h; | 95% |
With triphenyl phosphite; hydrogen In chloroform at 25℃; Rate constant; Mechanism; | |
With hydrogen; palladium on activated charcoal In ethanol; trifluoroacetic acid for 24h; Hydrogenation; |
Conditions | Yield |
---|---|
With dmap In dichloromethane at 20℃; for 2h; | 97% |
With dmap; triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 89% |
With pyridine | |
With triethylamine In dichloromethane |
4-allylpyrocatechol
benzyl bromide
3-[3,4-bis(benzyloxy)phenyl]prop-1-ene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2.5h; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
Stage #1: 4-allylpyrocatechol With carbonate salt In acetone Inert atmosphere; Stage #2: propargyl bromide In acetone Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
Stage #1: d(4)-methanol With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0℃; for 0.0833333h; Stage #2: 4-allylpyrocatechol In tetrahydrofuran at 0 - 20℃; for 0.5h; Mitsunobu Displacement; Inert atmosphere; | 86% |
4-allylpyrocatechol
tert-butyldimethylsilyl chloride
((4-allyl-1,2-phenylene)bis(oxy))bis(tert-butyldimethylsilane)
Conditions | Yield |
---|---|
With 1H-imidazole; dmap In N,N-dimethyl-formamide at 0 - 20℃; for 4h; Inert atmosphere; | 81% |
With 1H-imidazole; dmap In N,N-dimethyl-formamide at 0 - 25℃; for 16h; Inert atmosphere; | 75% |
With 1H-imidazole; dmap In dichloromethane at 0 - 20℃; | 63% |
4-allylpyrocatechol
santarubin B
Conditions | Yield |
---|---|
With air In methanol; acetonitrile at 80℃; for 10h; | 74% |
4-allylpyrocatechol
coniferal alcohol
C19H20O5
Conditions | Yield |
---|---|
With silver(l) oxide In acetone; benzene for 24h; hetero-Diels-Alder reaction; | 73% |
4-allylpyrocatechol
bromoacetic acid methyl ester
dimethyl 2,2'-[(4-allyl-1,2-phenylene)-bis(oxy)]diacetate
Conditions | Yield |
---|---|
With sodium methylate In methanol for 16h; Williamson reaction; Heating; | 65% |
Conditions | Yield |
---|---|
61.3% | |
With potassium carbonate; sodium iodide In acetone for 4h; Heating; |
4-allylpyrocatechol
coniferol
6-allyl-3-(4-hydroxy-3-methoxyphenyl)-2-hydroxymethyl-1,4-benzodioxan
Conditions | Yield |
---|---|
In acetone; benzene for 20h; Ambient temperature; | 50% |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In methanol; hexane; acetonitrile at 0 - 20℃; | 46% |
4-allylpyrocatechol
3-(3',4'-dihydroxyphenyl)-1-propanol
Conditions | Yield |
---|---|
Stage #1: 4-allylpyrocatechol With dimethylsulfide borane complex In tetrahydrofuran at -10 - 20℃; for 1.25h; Inert atmosphere; Stage #2: With sodium perborate hexahydrate In tetrahydrofuran; water at 20℃; for 2h; | 35.1% |
4-allylpyrocatechol
allyl bromide
A
4-allyl-5-propylbenzene-1,2-diol
B
3-allyl-4-propylbenzene-1,2-diol
Conditions | Yield |
---|---|
Stage #1: 4-allylpyrocatechol With potassium carbonate In acetone for 1.5h; Stage #2: allyl bromide In acetone Reflux; | A 15% B 20.58% |
Conditions | Yield |
---|---|
With potassium carbonate; acetone |
4-allylpyrocatechol
4-allylpyrocatechol
benzyl chloride
3-[3,4-bis(benzyloxy)phenyl]prop-1-ene
Conditions | Yield |
---|---|
With potassium carbonate; acetone |
Conditions | Yield |
---|---|
With alkali |
4-allylpyrocatechol
chloroacetic acid
(5-allyl-2-hydroxy-phenoxy)-acetic acid
Conditions | Yield |
---|---|
With potassium hydroxide |
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