1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime

Base Information

Chemical Name:1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime
CAS No.:87736-81-0
Molecular Formula:C₂₀H₂₂F₃NO₄S
Molecular Weight:429.46
Hs Code.:

Synonyms:1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime

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Chemical Property of 1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime

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Technology Process of 1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime

There total 6 articles about 1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime 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: 87.0%

: 87736-78-5
1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone oxime

: 98-59-9
p-toluenesulfonyl chloride

: 87736-81-0
1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime

Guidance literature:: In pyridine; for 3h; Heating;

Reference yield:

: 873-75-6
4-bromobenzenemethanol

: 87736-81-0
1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime

Guidance literature:: Multi-step reaction with 4 steps

1: 54 percent / conc. H₂SO₄ / CH₂Cl₂

2: 1) n-BuLi / 1) hexane, ether, -30 to 0 deg C in 2 h, 2) ether, -50 deg C, 3 h

3: 57 percent / NH₃OHCl, NaOH / ethanol / 16 h / Heating

4: 87 percent / pyridine / 3 h / Heating

With sodium hydroxide; n-butyllithium; hydroxylamine hydrochloride; sulfuric acid; In pyridine; ethanol; dichloromethane;

Reference yield:

: 22807-80-3
1-bromo-4-(tert-butoxymethyl)benzene

: 87736-81-0
1-<(4-tert-butoxymethyl)phenyl>-2,2,2-trifluoro-1-ethanone O-(p-tolylsulfonyl)oxime

Guidance literature:: Multi-step reaction with 3 steps

1: 1) n-BuLi / 1) hexane, ether, -30 to 0 deg C in 2 h, 2) ether, -50 deg C, 3 h

2: 57 percent / NH₃OHCl, NaOH / ethanol / 16 h / Heating

3: 87 percent / pyridine / 3 h / Heating

With sodium hydroxide; n-butyllithium; hydroxylamine hydrochloride; In pyridine; ethanol;