(3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole

Base Information

Chemical Name:(3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole
CAS No.:136173-06-3
Molecular Formula:C₁₃H₁₇NO₂
Molecular Weight:219.283
Hs Code.:

Synonyms:(3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole

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Chemical Property of (3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole

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Technology Process of (3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole

There total 1 articles about (3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole 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:

: 469-22-7
eseroline

: 136173-06-3
(3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole

Guidance literature:: Multi-step reaction with 2 steps

1: KOH / dimethylsulfoxide / 2 h / Ambient temperature

2: 7 N NaOH / 6 h / Heating

With potassium hydroxide; sodium hydroxide; In dimethyl sulfoxide;
DOI:10.1002/hlca.19910740409

Reference yield:

: 136173-06-3
(3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole

: 136092-41-6
(-)-5-O-(phenylcarbamoyl)physovenol

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / BBr₃ / CH₂Cl₂ / 2 h / Ambient temperature

2: 1) Na / 1) Et₂O, rt, 2) rt

With sodium; boron tribromide; In dichloromethane;
DOI:10.1002/hlca.19910740409

Reference yield:

: 136173-06-3
(3aS,8aS)-5-methoxy-3a,8-dimethyl-3,3a,8,8a-tetrahydro-2H-furo[2,3-b]indole

: 136092-42-7
(-)-5-O-(cumylcarbamoyl)physovenol

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / BBr₃ / CH₂Cl₂ / 2 h / Ambient temperature

2: 1) Na / 1) Et₂O, rt, 2) rt

With sodium; boron tribromide; In dichloromethane;
DOI:10.1002/hlca.19910740409