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2-methyl-3-nitro-benzaldehyde dimethylacetal

Base Information Edit
  • Chemical Name:2-methyl-3-nitro-benzaldehyde dimethylacetal
  • CAS No.:76499-33-7
  • Molecular Formula:C10H13NO4
  • Molecular Weight:211.218
  • Hs Code.:
  • Mol file:76499-33-7.mol
2-methyl-3-nitro-benzaldehyde dimethylacetal

Synonyms:2-methyl-3-nitro-benzaldehyde dimethylacetal

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Chemical Property of 2-methyl-3-nitro-benzaldehyde dimethylacetal Edit
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Technology Process of 2-methyl-3-nitro-benzaldehyde dimethylacetal

There total 2 articles about 2-methyl-3-nitro-benzaldehyde dimethylacetal 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:
Guidance literature:
With thionyl chloride; 1.) dry ice/ethanol bath, 2.) room temp., 1 h;
DOI:10.1021/jo00321a053
Guidance literature:
Multi-step reaction with 2 steps
1: 52.5 percent / CrO3, H2SO4, AcOH / 0.5 h / 5 - 10 °C
2: 95 percent / thionyl chloride / 1.) dry ice/ethanol bath, 2.) room temp., 1 h
With chromium(VI) oxide; thionyl chloride; sulfuric acid; acetic acid;
DOI:10.1021/jo00321a053
Guidance literature:
Multi-step reaction with 6 steps
1: H2O
2: 96.5 percent / BF3*Et2O / CHCl3 / 0.5 h / Ambient temperature
3: 1) pyrrolidine, 2) hydrazine hydrate / 2) Raney-Ni / 1) DMF, 135 deg C, 3h, 2) THF/MeOH, 2-propanol, 50 deg C, 3h
4: 1) NaOMe / 1) Et2O, 1h, 2) overnight, r.t.
5: 120 mg / H2 / Pd/C / methanol; CH2Cl2 / 0.75 h / 760 Torr / Ambient temperature
6: 89 percent / NaBH4 / 1) r.t., 1h, 2) 60 - 70 deg C
With pyrrolidine; sodium tetrahydroborate; water; hydrogen; sodium methylate; hydrazine hydrate; palladium on activated charcoal; boron trifluoride diethyl etherate; nickel; In methanol; dichloromethane; chloroform;
DOI:10.1002/ardp.19903230305
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