(3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol

Base Information

Chemical Name:(3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol
CAS No.:122504-59-0
Molecular Formula:C₂₁H₁₉ClO₃
Molecular Weight:354.833
Hs Code.:

Synonyms:(3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol

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Technology Process of (3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol

There total 1 articles about (3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol 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:

: 106-39-8
bromochlorobenzene

: 2426-87-1
3-methoxy-4-(phenylmethoxy)benzaldehyde

: 122504-59-0
(3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol

Guidance literature:: With magnesium; Yield given. Multistep reaction; 1.) ether, 2.) reflux, 2 h;
DOI:10.1002/ardp.19893220606

Reference yield:

: 122504-59-0
(3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol

: 134612-27-4
(3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanone

Guidance literature:

Reference yield:

: 122504-59-0
(3-methoxyl-4-benzyloxyl phenyl)(4-chlorophenyl)methanol

: 1620077-28-2
C₂₁H₁₈ClNO₃

Guidance literature:: Multi-step reaction with 2 steps

1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / dimethyl sulfoxide / 4 h / 20 °C

2: sodium hydroxide; hydroxylamine hydrochloride / ethanol / 6 h / Reflux

With hydroxylamine hydrochloride; sodium hydroxide; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In ethanol; dimethyl sulfoxide;
DOI:10.1039/c4ob00744a