1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

Base Information

Chemical Name:1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
CAS No.:79624-69-4
Molecular Formula:C₃₈H₃₇NO₄*ClH
Molecular Weight:608.177
Hs Code.:

Synonyms:1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

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Chemical Property of 1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

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Technology Process of 1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

There total 4 articles about 1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride 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: 84.0%

: 79624-63-8
1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-3,4-dihydroisoquinoline hydrochloride

: 79624-69-4
1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

Guidance literature:: With sodium tetrahydroborate; In methanol; at 20 ℃; for 0.5h;
DOI:10.1039/P19810002030

Reference yield:

: 39188-62-0
2-(4-(benzyloxy)phenyl)acetyl chloride

: 79624-69-4
1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogen carbonate / CH₂Cl₂; H₂O / 1 h

2: phosphorus oxychloride / acetonitrile / 0.33 h / Heating

3: 84 percent / sodium borohydride / methanol / 0.5 h / 20 °C

With sodium tetrahydroborate; sodium hydrogencarbonate; trichlorophosphate; In methanol; dichloromethane; water; acetonitrile;
DOI:10.1039/P19810002030

Reference yield:

: 6547-53-1
2-[4-(benzyloxy)benzyl]acetic acid

: 79624-69-4
1-(4-benzyloxybenzyl)-6,7-bisbenzyloxy-8-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: oxalyl chloride, DMF / benzene / 0.5 h

2: sodium hydrogen carbonate / CH₂Cl₂; H₂O / 1 h

3: phosphorus oxychloride / acetonitrile / 0.33 h / Heating

4: 84 percent / sodium borohydride / methanol / 0.5 h / 20 °C

With sodium tetrahydroborate; oxalyl dichloride; sodium hydrogencarbonate; N,N-dimethyl-formamide; trichlorophosphate; In methanol; dichloromethane; water; acetonitrile; benzene;
DOI:10.1039/P19810002030