(R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:(R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline
CAS No.:182056-10-6
Molecular Formula:C₃₃H₃₅NO₃
Molecular Weight:493.646
Hs Code.:

Synonyms:(R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

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Chemical Property of (R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

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Technology Process of (R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

There total 7 articles about (R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-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:

: 182056-05-9
1-(3-Benzyloxy-benzyl)-6,7-dimethoxy-2-((R)-1-phenyl-ethyl)-3,4-dihydro-isoquinolinium

: 182056-10-6
(R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With sodium tetrahydroborate; In methanol; at -78 ℃; for 2h; Yield given;

Reference yield:

: 93-40-3
(3,4-Dimethoxyphenyl)acetic acid

: 182056-10-6
(R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 6 steps

1: SOCl₂

2: 97.8 percent / 5percent aq. Na₂CO₃ / diethyl ether / 1 h / 0 - 5 °C

3: BF₃*OEt₂, BH₃ / tetrahydrofuran / 2.5 h / Heating

4: 87.2 percent / 5percent aq. NaOH / diethyl ether / 2 h / 0 - 5 °C

5: 5.0 g / POCl₃ / toluene / 3.5 h / Heating

6: NaBH₄ / methanol / 2 h / -78 °C

With sodium hydroxide; sodium tetrahydroborate; thionyl chloride; boron trifluoride diethyl etherate; borane; sodium carbonate; trichlorophosphate; In tetrahydrofuran; methanol; diethyl ether; toluene;

Reference yield:

: 1860-58-8
3-benzyloxyphenylacetic acid

: 182056-10-6
(R)-1-(3-benzyloxybenzyl)-N-((1R)-phenylethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂

2: 87.2 percent / 5percent aq. NaOH / diethyl ether / 2 h / 0 - 5 °C

3: 5.0 g / POCl₃ / toluene / 3.5 h / Heating

4: NaBH₄ / methanol / 2 h / -78 °C

With sodium hydroxide; sodium tetrahydroborate; thionyl chloride; trichlorophosphate; In methanol; diethyl ether; toluene;