(1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one

Base Information

Chemical Name:(1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one
CAS No.:1353669-96-1
Molecular Formula:C₂₈H₃₄O₅
Molecular Weight:450.575
Hs Code.:

Synonyms:(1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one

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Chemical Property of (1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one

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Technology Process of (1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one

There total 3 articles about (1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-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: 90.0%

: (1R,2S,3R,4S,8aR)-2,3-bis(benzyloxy)-4-hydroxy-8-iodo-4-propyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-1-yl formate

: 1353669-94-9
(1R,2S,3R,4S,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-1-yl formate

: 1353669-96-1
(1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; Inert atmosphere; Reflux;
DOI:10.1002/ejoc.201100815

Reference yield:

: 1018784-63-8
C₂₈H₃₂O₅

: 1353669-94-9
(1R,2S,3R,4S,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-1-yl formate

: 1353669-96-1
(1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / 80 °C / Inert atmosphere

2.1: diisobutylaluminium hydride / hexane; dichloromethane / -78 °C / Inert atmosphere

2.2: Inert atmosphere

3.1: [bis(acetoxy)iodo]benzene; iodine / cyclohexane / Inert atmosphere

4.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / benzene / Inert atmosphere; Reflux

With 2,2'-azobis(isobutyronitrile); [bis(acetoxy)iodo]benzene; iodine; tri-n-butyl-tin hydride; diisobutylaluminium hydride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In hexane; dichloromethane; cyclohexane; benzene;
DOI:10.1002/ejoc.201100815

Reference yield:

: 1367876-75-2
C₂₈H₃₂O₅

: 1353669-94-9
(1R,2S,3R,4S,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-1-yl formate

: 1353669-96-1
(1R,2S,3R,4S,4aS,8aR)-2,3-bis(benzyloxy)-4-hydroxy-4-propyl-octahydro-1H-1,4a-(epoxymethano)naphthalen-9-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisobutylaluminium hydride / hexane; dichloromethane / -78 °C / Inert atmosphere

1.2: Inert atmosphere

2.1: [bis(acetoxy)iodo]benzene; iodine / cyclohexane / Inert atmosphere

3.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / benzene / Inert atmosphere; Reflux

With 2,2'-azobis(isobutyronitrile); [bis(acetoxy)iodo]benzene; iodine; tri-n-butyl-tin hydride; diisobutylaluminium hydride; In hexane; dichloromethane; cyclohexane; benzene;
DOI:10.1002/ejoc.201100815