(1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Base Information

Chemical Name:(1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
CAS No.:286459-64-1
Molecular Formula:C₂₉H₃₁NO₄
Molecular Weight:457.569
Hs Code.:

Synonyms:(1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

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Chemical Property of (1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

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Technology Process of (1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

There total 4 articles about (1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid 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%

: 1700-31-8
3-benzyloxybenzyl bromide

: 116174-79-9
(3S)-1,2,3,4-tetrahydro-2-pivaloylisoquinoline-3-carboxylic acid

: 286459-64-1
(1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Guidance literature:: With tert.-butyl lithium; In tetrahydrofuran; pentane; at -78 ℃; for 72h;
DOI:10.1002/ejoc.200300175

Reference yield:

: 3282-30-2
pivaloyl chloride

: 286459-64-1
(1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / Et₃N

2: 99 percent / hydrogen / Pd/C

3: 84 percent / t-BuLi / pentane; tetrahydrofuran / 72 h / -78 °C

With hydrogen; tert.-butyl lithium; triethylamine; palladium on activated charcoal; In tetrahydrofuran; pentane;
DOI:10.1002/ejoc.200300175

Reference yield:

: 77497-96-2
(S)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid, phenylmethylester

: 286459-64-1
(1R,3S)-1-(m-benzyloxybenzyl)-2-pivaloyl-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / Et₃N

2: 99 percent / hydrogen / Pd/C

3: 84 percent / t-BuLi / pentane; tetrahydrofuran / 72 h / -78 °C

With hydrogen; tert.-butyl lithium; triethylamine; palladium on activated charcoal; In tetrahydrofuran; pentane;
DOI:10.1002/ejoc.200300175