tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate

Base Information

Chemical Name:tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate
CAS No.:1609671-74-0
Molecular Formula:C₂₂H₂₃F₃N₂O₄
Molecular Weight:436.431
Hs Code.:

Synonyms:tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate

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Chemical Property of tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate

Chemical Property:

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Technology Process of tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate

There total 3 articles about tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate 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:

: 66493-39-8
4-(N-tert-butoxycarbonyl)aminobenzoic acid

: 1388072-38-5
3-(3-(trifluoromethyl)phenyl)azetidin-3-ol

: 1609671-74-0
tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 1609671-73-9
tert-butyl 3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carboxylate

: 1609671-74-0
tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

2: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 401-78-5
3-bromo-1-trifluoromethylbenzene

: 1609671-74-0
tert-butyl 4-(3-hydroxy-3-(3-(trifluoromethyl)phenyl)azetidine-1-carbonyl)phenylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran / 0.5 h / -78 °C

1.2: 2 h / -78 °C / Inert atmosphere

2.1: hydrogenchloride / 1,4-dioxane / 2 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; n-butyllithium; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;