1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone

Base Information

Chemical Name:1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone
CAS No.:118683-66-2
Molecular Formula:C₂₀H₂₂N₄O₄
Molecular Weight:382.419
Hs Code.:

Synonyms:1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone

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Chemical Property of 1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone

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Technology Process of 1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone

There total 4 articles about 1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone 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:

: 4-(4-Acetyl-3-hydroxy-2-propyl-phenoxymethyl)-3-methoxy-benzonitrile

: 118683-66-2
1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone

Guidance literature:: With sodium azide; ammonium chloride; In N,N-dimethyl-formamide; at 120 ℃; for 48h;

Reference yield:

: 40786-69-4
1-(2,4-dihydroxy-3-propylphenyl)ethanone

: 118683-66-2
1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / Heating

2: NaN₃, NH₄Cl / dimethylformamide / 48 h / 120 °C

With sodium azide; potassium carbonate; ammonium chloride; In N,N-dimethyl-formamide; acetone;

Reference yield:

: 3556-60-3
3-methoxy-4-methylcyano-benzene

: 118683-66-2
1-{2-Hydroxy-4-[2-methoxy-4-(1H-tetrazol-5-yl)-benzyloxy]-3-propyl-phenyl}-ethanone

Guidance literature:: Multi-step reaction with 3 steps

1: N-bromosuccinimide, benzoyl peroxide / CCl₄ / 0.5 h / Heating; Irradiation

2: K₂CO₃ / acetone / Heating

3: NaN₃, NH₄Cl / dimethylformamide / 48 h / 120 °C

With N-Bromosuccinimide; sodium azide; Perbenzoic acid; potassium carbonate; ammonium chloride; In tetrachloromethane; N,N-dimethyl-formamide; acetone;