1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester

Base Information

Chemical Name:1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester
CAS No.:114692-73-8
Molecular Formula:C₃₂H₄₃F₆NO₄
Molecular Weight:619.688
Hs Code.:

Synonyms:1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester

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Chemical Property of 1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester

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Technology Process of 1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester

There total 2 articles about 1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester 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: 26.0%

: 114692-69-2
1,7,8-Tri-tert-butyl-3-(4-methoxyphenyl)-5,5-bis(trifluormethyl)-2-oxa-4-azabicyclo<4.2.0>octa-3,7-dien-6-carbonsaeure-tert-butylester

: 114692-73-8
1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester

Guidance literature:: With trifluoroacetic acid; In chloroform; at 55 ℃; for 48h;

Reference yield:

: 40024-23-5
4-methoxy-N-(2,2,2-trifluoro-1-trifluoromethyl-ethylidene)-benzamide

: 114692-73-8
1,5,6-Tri-tert-butyl-2-(4-methoxybenzoyl)-3,3-bis(trifluormethyl)-2-azabicyclo<2.2.0>hex-5-en-4-carbonsaeure-tert-butylester

Guidance literature:: Multi-step reaction with 2 steps

1: 59 percent / pentane / 22 h / 20 °C

2: 26 percent / TFA / CHCl₃ / 48 h / 55 °C

With trifluoroacetic acid; In chloroform; pentane;