6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

Base Information

Chemical Name:6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one
CAS No.:172937-49-4
Molecular Formula:C₂₈H₂₆N₂O₂
Molecular Weight:422.527
Hs Code.:

6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2<i>H</i>-pyridazin-3-one

Synonyms:6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

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Chemical Property of 6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

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Technology Process of 6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

There total 8 articles about 6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one 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: 83.0%

: 172937-44-9
6-benzhydryl-2-(5-methoxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

: 172937-49-4
6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

Guidance literature:: With boron tribromide; In dichloromethane; Heating;
DOI:10.1016/S0960-894X(00)00571-0

Reference yield:

: 328553-17-9
(1R,2S)-methyl [1-hydroxy-5-methoxy-1,2,3,4-tetrahydro-2-naphthyl]formate

: 172937-49-4
6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 5 steps

1: H₂ / 10 percent Pd/C / methanol / 20 °C / 2280 Torr

2: 99 percent / LiAlH₄ / tetrahydrofuran / -70 °C

3: Et₃N / CH₂Cl₂ / 0 °C

4: t-BuOK; 18-crown-6 / dimethylformamide / 20 °C

5: 83 percent / BBr₃ / CH₂Cl₂ / Heating

With lithium aluminium tetrahydride; 18-crown-6 ether; potassium tert-butylate; hydrogen; boron tribromide; triethylamine; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(00)00571-0

Reference yield:

: 781-35-1
1,1-diphenylacetone

: 172937-49-4
6-benzhydryl-2-(5-hydroxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl)-2H-pyridazin-3-one

Guidance literature:: Multi-step reaction with 4 steps

1: H₂O / 1,2-dimethoxy-ethane / 72 h / Heating

2: NH₂NH₂*H₂O / H₂O / Heating

3: t-BuOK; 18-crown-6 / dimethylformamide / 20 °C

4: 83 percent / BBr₃ / CH₂Cl₂ / Heating

With 18-crown-6 ether; potassium tert-butylate; water; boron tribromide; hydrazine hydrate; In 1,2-dimethoxyethane; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(00)00571-0