(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

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Chemical Name:(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one
CAS No.:142133-46-8
Molecular Formula:C₂₂H₂₆O₅
Molecular Weight:370.445
Hs Code.:

Synonyms:(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

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Chemical Property of (4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

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Technology Process of (4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

There total 1 articles about (4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one 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:

: 186581-53-3,908094-01-9,334-88-3
diazomethane

: 142133-30-0
(1R,2R,3S,8R,10S,11S,13R)-10-(benzyloxy)-6-hydroxy-15,15-dimethyl-12,14,16-trioxatetracyclo<11.3.0.0^2,11.0^3,8>hexadec-5-en-4-one

: 142133-47-9
(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-decahydro-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

: 142133-46-8
(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

Guidance literature:: Yield given. Multistep reaction. Yields of byproduct given;
DOI:10.1021/jo00042a034

Reference yield: 79.0%

: 142133-46-8
(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

: 142133-47-9
(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-decahydro-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

Guidance literature:: With hydrogen; nickel;
DOI:10.1021/jo00042a034

Reference yield:

: 142133-46-8
(4aS,6S,6aS,7aR,10aR,10bR,10cS)-6-Benzyloxy-9,9-dimethyl-4a,5,6,6a,7a,10a,10b,10c-octahydro-4H-7,8,10-trioxa-pentaleno[1,2-a]naphthalen-1-one

: 142235-10-7
C₂₂H₂₈O₆

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / hydrogen / nickel

2: 78 percent / m-chloroperbenzoic acid

With hydrogen; 3-chloro-benzenecarboperoxoic acid; nickel;
DOI:10.1021/jo00042a034