3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde

Base Information

Chemical Name:3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde
CAS No.:250284-72-1
Molecular Formula:C₂₀H₂₁BrO₅
Molecular Weight:421.288
Hs Code.:

Synonyms:3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde

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Chemical Property of 3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde

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Technology Process of 3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde

There total 6 articles about 3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 76.0%

: 129866-90-6
2,2'-dimethoxy-5,5'-diformyl-diphenyl-iodonium bromide

: 250284-68-5
2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenol

: 2314-37-6
3-iodo-4-methoxybenzaldehyde

: 250284-72-1
3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 90 ℃;
DOI:10.1016/S0040-4039(99)01429-X

Reference yield:

: 6793-92-6
p-benzyloxyphenylbromide

: 250284-72-1
3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde

Guidance literature:: Multi-step reaction with 6 steps

1: 93 percent / Mg / tetrahydrofuran / Heating

2: 99 percent / K₂OsO₂(OH)2; K₂CO₃; K₃Fe(CN)6 / 2-methyl-propan-2-ol; H₂O / 20 °C

3: 95 percent / 2,2-dimethoxypropane; PPTS / 20 °C

4: 99 percent / hydrogen / 10 percent Pd/C / ethyl acetate / 20 °C

5: 87 percent / NBS / dimethylformamide / 20 °C

6: 76 percent / NaH / dimethylformamide / 90 °C

With N-Bromosuccinimide; K₂OsO₂(OH)2; hydrogen; pyridinium p-toluenesulfonate; sodium hydride; potassium carbonate; magnesium; 2,2-dimethoxy-propane; potassium hexacyanoferrate(III); palladium on activated charcoal; In tetrahydrofuran; water; ethyl acetate; N,N-dimethyl-formamide; tert-butyl alcohol; 1: Alkylation / 2: Oxidation / 3: acetonization / 4: Reduction / 5: Bromination / 6: Arylation;
DOI:10.1016/S0040-4039(99)01429-X

Reference yield:

: 90617-59-7
1-(benzyloxy)-4-(prop-2-en-1-yl)benzene

: 250284-72-1
3-[2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenoxy]-4-methoxy-benzaldehyde

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / K₂OsO₂(OH)2; K₂CO₃; K₃Fe(CN)6 / 2-methyl-propan-2-ol; H₂O / 20 °C

2: 95 percent / 2,2-dimethoxypropane; PPTS / 20 °C

3: 99 percent / hydrogen / 10 percent Pd/C / ethyl acetate / 20 °C

4: 87 percent / NBS / dimethylformamide / 20 °C

5: 76 percent / NaH / dimethylformamide / 90 °C

With N-Bromosuccinimide; K₂OsO₂(OH)2; hydrogen; pyridinium p-toluenesulfonate; sodium hydride; potassium carbonate; 2,2-dimethoxy-propane; potassium hexacyanoferrate(III); palladium on activated charcoal; In water; ethyl acetate; N,N-dimethyl-formamide; tert-butyl alcohol; 1: Oxidation / 2: acetonization / 3: Reduction / 4: Bromination / 5: Arylation;
DOI:10.1016/S0040-4039(99)01429-X