(-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol

Base Information

Chemical Name:(-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol
CAS No.:403706-15-0
Molecular Formula:C₂₅H₃₀O₆
Molecular Weight:426.51
Hs Code.:

Synonyms:(-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol

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Chemical Property of (-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol

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Technology Process of (-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol

There total 9 articles about (-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol 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: 94.0%

: 403706-14-9
(+)-(2R,3R)-toluene-4-sulfonic acid 3-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-2,3-oxiranylmethyl ester

: 403706-15-0
(-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃; for 2.5h;
DOI:10.1021/jo0611364

Reference yield:

: 403706-13-8
(+)-(2R,3R)-{3-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-2,3-oxiranyl}methanol

: 403706-15-0
(-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / Et₃N; DMAP / CH₂Cl₂ / 1 h / 0 °C

2: 94 percent / LiAlH₄ / tetrahydrofuran / 2.5 h / 0 - 20 °C

With dmap; lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo0611364

Reference yield:

: 22273-56-9
4-hydroxy-5-methoxy-2-methyl-naphthalene

: 403706-15-0
(-)-(2R)-1-(3,5-dimethoxy-4-(8-methoxy-1-methoxymethoxy-3-methylnaphthalen-2-yl)-phenyl)-propan-2-ol

Guidance literature:: Multi-step reaction with 7 steps

1.1: pyridine / CH₂Cl₂ / 24 h / 20 °C

1.2: 67 percent / aq. HCl / 1 h

2.1: 81 percent / NaH / tetrahydrofuran / 20 °C

3.1: NaH / benzene / 0.25 h / 0 °C

3.2: 100 percent / benzene / 1.5 h / 0 - 20 °C

4.1: 89 percent / DIBAL-H / toluene / 0.25 h / -78 °C

5.1: 63 percent / Ti(O-iPr)4; diisopropyl-D-tartrate; t-BuOOH / CH₂Cl₂ / 5 h / -20 °C

6.1: 83 percent / Et₃N; DMAP / CH₂Cl₂ / 1 h / 0 °C

7.1: 94 percent / LiAlH₄ / tetrahydrofuran / 2.5 h / 0 - 20 °C

With pyridine; titanium(IV) isopropylate; tert.-butylhydroperoxide; dmap; lithium aluminium tetrahydride; sodium hydride; diisobutylaluminium hydride; D-(-)-diisopropyl tartrate; triethylamine; In tetrahydrofuran; dichloromethane; toluene; benzene; 3.2: Horner-Wadsworth-Emmons reaction / 5.1: Katsuki-Sharpless asymmetric epoxidation;
DOI:10.1021/jo0611364