[(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine

Base Information

Chemical Name:[(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine
CAS No.:606970-28-9
Molecular Formula:C₃₆H₃₉NO₅
Molecular Weight:565.709
Hs Code.:

Synonyms:[(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine

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Chemical Property of [(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine

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Technology Process of [(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine

There total 3 articles about [(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine 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: 66.0%

: 1826-67-1
vinyl magnesium bromide

: 606970-28-9
[(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine

Guidance literature:: In diethyl ether; at 0 - 20 ℃; for 24h;
DOI:10.1055/s-2003-41465

Reference yield:

: 2018-90-8
naphthalen-2-ylmethylamine

: 606970-28-9
[(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 2 h / 4 °C

2: diethyl ether / 24 h / 0 - 20 °C

In diethyl ether; dichloromethane;
DOI:10.1021/ol035117h

Reference yield:

: 302788-33-6
3,6-di-O-benzyl-4,5-O-isopropylidene-D-xylo-aldehydo-hexos-5-ulo-2,5-furanose

: 606970-28-9
[(R)-1-((3aS,5S,6R,6aS)-6-Benzyloxy-3a-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-allyl]-naphthalen-2-ylmethyl-amine

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 2 h / 4 °C

2: diethyl ether / 24 h / 0 - 20 °C

In diethyl ether; dichloromethane;
DOI:10.1021/ol035117h