1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole

Base Information

• Chemical Name: 1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole
• CAS No.: 113801-61-9
• Molecular Formula: C₂₉H₃₅NO₃S
• Molecular Weight: 477.668

Synonyms:1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole

Chemical Property of 1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole

Chemical Property:

Purity/Quality:

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Technology Process of 1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole

There total 4 articles about 1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-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: 95.0%

(6E,10E)-12-(1-Benzenesulfonyl-1H-indol-2-yl)-3-bromo-2,6,10-trimethyl-dodeca-6,10-dien-2-ol (113801-59-5) → 1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole (113801-61-9)

Guidance literature:

With potassium carbonate; In methanol; for 1h; Ambient temperature;

DOI:10.1016/S0040-4039(00)95537-0

Reference yield:

1-benzenesulfonylindole (40899-71-6) → 1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole (113801-61-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 70 percent

2: NBS

3: 95 percent / K₂CO₃ / methanol / 1 h / Ambient temperature

With N-Bromosuccinimide; potassium carbonate; In methanol;

DOI:10.1016/S0040-4039(00)95537-0

Reference yield:

farnesyl bromide (24163-93-7,24163-94-8,56881-57-3,6874-67-5,28290-41-7) → 1-Benzenesulfonyl-2-[(2E,6E)-9-(3,3-dimethyl-oxiranyl)-3,7-dimethyl-nona-2,6-dienyl]-1H-indole (113801-61-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 70 percent

2: NBS

3: 95 percent / K₂CO₃ / methanol / 1 h / Ambient temperature

With N-Bromosuccinimide; potassium carbonate; In methanol;

DOI:10.1016/S0040-4039(00)95537-0

upstream raw materials:

(6E,10E)-12-(1-Benzenesulfonyl-1H-indol-2-yl)-3-bromo-2,6,10-trimethyl-dodeca-6,10-dien-2-ol

1-benzenesulfonylindole

farnesyl bromide

1-Benzenesulfonyl-2-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-1H-indole

Downstream raw materials:

1-Benzenesulfonyl-2-[(E)-3-methyl-5-((1R,4S)-1,3,3-trimethyl-7-oxa-bicyclo[2.2.1]hept-2-yl)-pent-2-enyl]-1H-indole

(3S,6aR,12bR)-11-Benzenesulfonyl-4,4,6a,12b-tetramethyl-1,2,3,4,4a,5,6,6a,11,12,12a,12b-dodecahydro-11-aza-benzo[5,6]pentaleno[2,1-b]naphthalen-3-ol

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