1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline
CAS No.:99612-81-4
Molecular Formula:C₃₂H₃₂N₂O₆
Molecular Weight:540.616
Hs Code.:

Synonyms:1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Suppliers and Price of 1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

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Chemical Property of 1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

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Technology Process of 1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

There total 4 articles about 1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline 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: 81.0%

: 99612-79-0
1-<5-benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-3,4-dihydroisoquinoline

: 99612-81-4
1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With sodium tetrahydroborate; In methanol; for 2h; Ambient temperature;

Reference yield:

: 99613-09-9
N-<4-Benzyloxy-4-methoxyphenethyl>-5-benzyloxy-4-methoxy-2-nitrophenylacetamide

: 99612-81-4
1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / POCl₃ / acetonitrile / 2 h / Heating

2: 81 percent / NaBH₄ / methanol / 2 h / Ambient temperature

With sodium tetrahydroborate; trichlorophosphate; In methanol; acetonitrile;

Reference yield:

: 78792-73-1
5-benzyloxy-4-methoxy-2-nitrophenylacetic acid

: 99612-81-4
1-<5-Benzyloxy-4-methoxy-2-nitrobenzyl>-7-benzyloxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 56 percent / 2 N NaOH / CHCl₃; H₂O / 4 h / Ambient temperature

2: 72 percent / POCl₃ / acetonitrile / 2 h / Heating

3: 81 percent / NaBH₄ / methanol / 2 h / Ambient temperature

With sodium hydroxide; sodium tetrahydroborate; trichlorophosphate; In methanol; chloroform; water; acetonitrile;