C₆₁H₇₃F₃N₂O₂₀

Base Information

Chemical Name:C₆₁H₇₃F₃N₂O₂₀
CAS No.:121042-81-7
Molecular Formula:C₆₁H₇₃F₃N₂O₂₀
Molecular Weight:1211.25
Hs Code.:

C<sub>61</sub>H<sub>73</sub>F<sub>3</sub>N<sub>2</sub>O<sub>20</sub>

Synonyms:C₆₁H₇₃F₃N₂O₂₀

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₆₁H₇₃F₃N₂O₂₀

Chemical Property:

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Technology Process of C₆₁H₇₃F₃N₂O₂₀

There total 7 articles about C₆₁H₇₃F₃N₂O₂₀ 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:

: 1125-88-8
benzaldehyde dimethyl acetal

: 121042-81-7
C₆₁H₇₃F₃N₂O₂₀

Guidance literature:: Multi-step reaction with 6 steps

1: 1) CH₃ONa, 2) toluene-4-sulfonic acid / 1) CH₃OH, 2 h, 2) CH₃CN, 50 deg C

2: pyridine / 20 h

3: NaBH₃CN, HCl / tetrahydrofuran; diethyl ether / 8 h / 20 °C / molecular sieve 3 Angstroem

4: CH₃ONa / methanol / 24 h

5: mercury cyanide / nitromethane; benzene / 2 h / 50 - 60 °C / molecular sieve 4 Angstroem

6: 1) ethyldiisopropylamine, (C₂H₅)4N⁽¹⁺⁾*Br^(1-) / 1) CH₂Cl₂, DMF, molecular sieve 4 Angstroem, 20 deg C, 15 h, 2) 96 h

With pyridine; hydrogenchloride; tetraethylammonium bromide; sodium methylate; mercury(II) cyanide; sodium cyanoborohydride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; diethyl ether; nitromethane; benzene;
DOI:10.1007/BF00598177

Reference yield:

: 121042-73-7
3-trifluoroacetamidopropyl 2-acetamido-6-O-benzyl-2-deoxy-β-D-glucopyranoside

: 121042-81-7
C₆₁H₇₃F₃N₂O₂₀

Guidance literature:: Multi-step reaction with 2 steps

1: mercury cyanide / nitromethane; benzene / 2 h / 50 - 60 °C / molecular sieve 4 Angstroem

2: 1) ethyldiisopropylamine, (C₂H₅)4N⁽¹⁺⁾*Br^(1-) / 1) CH₂Cl₂, DMF, molecular sieve 4 Angstroem, 20 deg C, 15 h, 2) 96 h

With tetraethylammonium bromide; mercury(II) cyanide; N-ethyl-N,N-diisopropylamine; In nitromethane; benzene;
DOI:10.1007/BF00598177

Reference yield:

: 121042-71-5
3-(trifluoroacetamido)propyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

: 121042-81-7
C₆₁H₇₃F₃N₂O₂₀

Guidance literature:: Multi-step reaction with 5 steps

1: pyridine / 20 h

2: NaBH₃CN, HCl / tetrahydrofuran; diethyl ether / 8 h / 20 °C / molecular sieve 3 Angstroem

3: CH₃ONa / methanol / 24 h

4: mercury cyanide / nitromethane; benzene / 2 h / 50 - 60 °C / molecular sieve 4 Angstroem

5: 1) ethyldiisopropylamine, (C₂H₅)4N⁽¹⁺⁾*Br^(1-) / 1) CH₂Cl₂, DMF, molecular sieve 4 Angstroem, 20 deg C, 15 h, 2) 96 h

With pyridine; hydrogenchloride; tetraethylammonium bromide; sodium methylate; mercury(II) cyanide; sodium cyanoborohydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; diethyl ether; nitromethane; benzene;
DOI:10.1007/BF00598177