(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

Base Information

Chemical Name:(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine
CAS No.:1242846-76-9
Molecular Formula:C₁₆H₁₈BrNO₂
Molecular Weight:336.228
Hs Code.:
Mol file:1242846-76-9.mol

Synonyms:(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

Suppliers and Price of (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

Chemical Property:

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

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Technology Process of (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

There total 5 articles about (4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine 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: 88.0%

: 937678-86-9
4-(4-methoxybenzyloxy)-3-bromobenzaldehyde

: 74-89-5
methylamine

: 1242846-76-9
(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

Guidance literature:: 4-(4-methoxybenzyloxy)-3-bromobenzaldehyde; methylamine; In methanol; at 20 ℃; for 0.5h;

With sodium tetrahydroborate; In methanol; at 20 ℃; for 1h;

Reference yield:

: C₁₆H₁₆BrNO₂

: 1242846-76-9
(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

Guidance literature:: With methanol; sodium tetrahydroborate; at 20 ℃; for 1h;

Reference yield:

: 2746-25-0
p-Methoxybenzyl bromide

: 1242846-76-9
(4-(4-methoxybenzyloxy)-3-bromophenyl)-N-methylmethanamine

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C

2: methanol / 0.5 h / 20 °C

3: sodium tetrahydroborate; methanol / 1 h / 20 °C

With methanol; sodium tetrahydroborate; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;