2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester

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Chemical Name:2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester
CAS No.:511257-14-0
Molecular Formula:C₂₆H₂₂Br₂N₂O₈
Molecular Weight:650.277
Hs Code.:

Synonyms:2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester

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Chemical Property of 2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester

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Technology Process of 2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester

There total 7 articles about 2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester 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: 91.0%

: 213382-45-7
5-bromo-4-fluoro-2-nitro-benzaldehyde

: 511257-13-9
2-[(E)-Benzyloxyimino]-3-(3-bromo-5-hydroxy-4-methoxy-phenyl)-propionic acid ethyl ester

: 511257-14-0
2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; for 4h;
DOI:10.1016/S0040-4039(02)02378-X

Reference yield:

: 16414-34-9
3-bromo-4,5-dihydroxybenzaldehyde

: 511257-14-0
2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: Li₂CO₃ / dimethylformamide / 4 h

2: K₂CO₃ / 2 h

3: 82 percent / NaHMDS / 0.5 h / -78 - 20 °C

4: HF-pyr / 10 h / 20 °C

5: 76 percent / RhCl₃*3H₂O / ethanol / 12 h / Heating

6: 91 percent / K₂CO₃ / dimethylformamide / 4 h

With pyridine; rhodium(III) chloride; hydrogen fluoride; sodium hexamethyldisilazane; lithium carbonate; potassium carbonate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(02)02378-X

Reference yield:

: 23354-30-5
3-bromo-4-methoxy-5-hydroxybenzaldehyde

: 511257-14-0
2-[(E)-Benzyloxyimino]-3-[3-bromo-5-(2-bromo-4-formyl-5-nitro-phenoxy)-4-methoxy-phenyl]-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: K₂CO₃ / 2 h

2: 82 percent / NaHMDS / 0.5 h / -78 - 20 °C

3: HF-pyr / 10 h / 20 °C

4: 76 percent / RhCl₃*3H₂O / ethanol / 12 h / Heating

5: 91 percent / K₂CO₃ / dimethylformamide / 4 h

With pyridine; rhodium(III) chloride; hydrogen fluoride; sodium hexamethyldisilazane; potassium carbonate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(02)02378-X