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Cas:122-73-6
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Cas:122-73-6
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Cas:122-73-6
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Cas:122-73-6
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Cas:122-73-6
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inquiryProduct Name: BENZYL ISOAMYL ETHER Synonyms: ether,benzylisopentyl;BENZYL ISOPENTYL ETHER;BENZYL ISOAMYL ETHER;BENZYL-3-METHYL BUTYL ETHER;GARDENIA ETHER;ISO-AMYL BENZYL ETHER;Benzyl lsoamyl Ether;isoamoxymethylbenzene CAS: 122-73-6 MF: C12H1
Cas:122-73-6
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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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Benzene,[(3-methylbutoxy)methyl]- cas 122-73-6Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
Cas:122-73-6
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Cas:122-73-6
Min.Order:10 Milligram
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FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the BENZYL ISOAMYL ETHER, CAS:122-73-6 with the most competitive price and the best quali
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(((3-methylbut-3-en-1-yl)oxy)methyl)benzene
((isopentyloxy)methyl)benzene
Conditions | Yield |
---|---|
With sodium tetrahydroborate; Hoveyda-Grubbs catalyst second generation In methanol; 1,2-dichloro-ethane for 18h; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
With hydrogenchloride; methylphenylsilane; 1,3-bis(4-cyano-3,5-bis(trifluoromethyl)phenyl)thiourea In 1,4-dioxane; dichloromethane at 20℃; for 2h; Molecular sieve; | 89% |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: sodium hydride / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere 1.2: 1 h / Inert atmosphere 2.1: Hoveyda-Grubbs catalyst second generation; sodium tetrahydroborate / 1,2-dichloro-ethane; methanol / 18 h / Inert atmosphere View Scheme |
benzaldehyde di(neopentyl) acetal
A
((isopentyloxy)methyl)benzene
B
α-isopropylcinnamaldehyde
C
benzaldehyde
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane 0 deg C to RT; | A 58% B 32% C 10% |
Conditions | Yield |
---|---|
With sulfuric acid at 125℃; | |
With sodium pyrosulfate |
benzaldehyde di(neopentyl) acetal
A
isoamyl benzoate
B
((isopentyloxy)methyl)benzene
C
benzaldehyde
Conditions | Yield |
---|---|
With monoaluminum phosphate at 300℃; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: HCl 2: diethyl ether View Scheme |
1-chloromethoxy-3-methyl-butane
((isopentyloxy)methyl)benzene
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With i-Amyl alcohol |
benzaldehyde di(neopentyl) acetal
A
isoamyl benzoate
B
((isopentyloxy)methyl)benzene
C
benzyl isovalerate
D
α-isopropyl cinnamaldehyde
E
benzaldehyde
F
benzyl alcohol
Conditions | Yield |
---|---|
With antimonypentachloride In 1,2-dichloro-ethane at 30℃; for 0.5h; Product distribution; Mechanism; action of Lewis acids, ferric chloride also used; |
i-Amyl alcohol
benzyl alcohol
A
isopentyl ether
B
dibenzyl ether
C
((isopentyloxy)methyl)benzene
Conditions | Yield |
---|---|
With hydrogenchloride; methylphenylsilane; 1,3-bis(4-cyano-3,5-bis(trifluoromethyl)phenyl)thiourea In 1,4-dioxane; dichloromethane at 20℃; for 2h; Molecular sieve; | 89% |
(((3-methylbut-3-en-1-yl)oxy)methyl)benzene
((isopentyloxy)methyl)benzene
Conditions | Yield |
---|---|
With sodium tetrahydroborate; Hoveyda-Grubbs catalyst second generation In methanol; 1,2-dichloro-ethane for 18h; Inert atmosphere; | 80% |
benzaldehyde di(neopentyl) acetal
A
((isopentyloxy)methyl)benzene
B
α-isopropylcinnamaldehyde
C
benzaldehyde
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane 0 deg C to RT; | A 58% B 32% C 10% |
1-chloromethoxy-3-methyl-butane
((isopentyloxy)methyl)benzene
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With i-Amyl alcohol |
benzaldehyde di(neopentyl) acetal
A
isoamyl benzoate
B
((isopentyloxy)methyl)benzene
C
benzaldehyde
Conditions | Yield |
---|---|
With monoaluminum phosphate at 300℃; Yield given. Yields of byproduct given; |
benzaldehyde di(neopentyl) acetal
A
isoamyl benzoate
B
((isopentyloxy)methyl)benzene
C
benzyl isovalerate
D
α-isopropyl cinnamaldehyde
E
benzaldehyde
F
benzyl alcohol
Conditions | Yield |
---|---|
With antimonypentachloride In 1,2-dichloro-ethane at 30℃; for 0.5h; Product distribution; Mechanism; action of Lewis acids, ferric chloride also used; |
i-Amyl alcohol
benzyl alcohol
A
isopentyl ether
B
dibenzyl ether
C
((isopentyloxy)methyl)benzene
Conditions | Yield |
---|---|
With sulfuric acid at 125℃; | |
With sodium pyrosulfate |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: HCl 2: diethyl ether View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: sodium hydride / N,N-dimethyl-formamide / 0.17 h / Inert atmosphere 1.2: 1 h / Inert atmosphere 2.1: Hoveyda-Grubbs catalyst second generation; sodium tetrahydroborate / 1,2-dichloro-ethane; methanol / 18 h / Inert atmosphere View Scheme |
((isopentyloxy)methyl)benzene
Conditions | Yield |
---|---|
In tetrahydrofuran; toluene at -10 - 20℃; for 6h; Acidic conditions; Cooling; | 46 mg |
((isopentyloxy)methyl)benzene
C12H16(2)H2O
Conditions | Yield |
---|---|
With hydrogen; water-d2; palladium on activated charcoal; ethylenediamine In tetrahydrofuran at 50℃; for 12h; | 93% |
With pyridine; hydrogen; water-d2; 5% Pd/C (en) at 50℃; for 12h; Product distribution / selectivity; | 89% |
With hydrogen; water-d2; triethylamine; 5% Pd/C (en) at 50℃; for 12h; Product distribution / selectivity; | 87% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; oxygen; N-ethyl-N,N-diisopropylamine at 80℃; for 24h; | 75% |
Conditions | Yield |
---|---|
With N-hydroxyphthalimide In pyridine anodic oxidation; | 65% |
Conditions | Yield |
---|---|
With tin(IV) chloride |
Conditions | Yield |
---|---|
With zinc(II) nitrate; silica gel In 2,2,4-trimethylpentane for 1h; Heating; | A 84 % Chromat. B 23 % Chromat. |
((isopentyloxy)methyl)benzene
tin(IV) chloride
benzene
A
i-Amyl alcohol
B
Diphenylmethane
C
1,4-dibenzylbenzene
Conditions | Yield |
---|---|
Behandeln mit Wasser; |
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