bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate

Base Information

Chemical Name:bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate
CAS No.:1407999-21-6
Molecular Formula:C₂₃H₂₂Cl₆N₂O₆
Molecular Weight:635.155
Hs Code.:

Synonyms:bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate

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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 bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate

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Technology Process of bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate

There total 1 articles about bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate 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: 85.0%

: 857839-66-8
4-phenylbutyl benzoate

: 38857-88-4
bis(2,2,2-trichlorethyl)azodicarboxylate

: 1407999-21-6
bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate

Guidance literature:: With N-hydroxyphthalimide; 1,1,1,3',3',3'-hexafluoro-propanol; at 60 ℃; for 3h; chemoselective reaction; Inert atmosphere;
DOI:10.1039/d1cc03466a

Reference yield: 77.0%

: 1407999-21-6
bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate

: 1407999-65-8
4-(benzoyloxy)-1-phenylbutylamine

Guidance literature:: bis(2,2,2-trichloroethyl) 1-[4-(benzoyloxy)-1-phenylbutyl]-1,2-hydrazinedicarboxylate; With acetic acid; zinc; at 20 ℃; Inert atmosphere;

In acetone; at 20 ℃; chemoselective reaction; Inert atmosphere;
DOI:10.1021/jo301840e