6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one

Base Information

Chemical Name:6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one
CAS No.:1434515-17-9
Molecular Formula:C₂₉H₄₇ClO₃Si₂
Molecular Weight:535.314
Hs Code.:

Synonyms:6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one

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Chemical Property of 6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one

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Technology Process of 6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one

There total 3 articles about 6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-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: 48.0%

: 1434515-11-3
6-(3-(2-chlorophenyl)allyl)-2,2,3,3,9,9,10,10-octamethyl-6-(prop-2-yn-1-yl)-4,8-dioxa-3,9-disilaundecane

: 78191-00-1
N-Methoxy-N-methylacetamide

: 1434515-17-9
6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one

Guidance literature:: With lithium diisopropyl amide; In tetrahydrofuran; n-heptane; ethylbenzene; at -78 - 20 ℃; for 5.25h; Inert atmosphere;
DOI:10.1021/ol400292q

Reference yield:

: 1395054-37-1
(E)-diethyl-2-(3-(2-chlorophenyl)allyl)-2-(prop-2-yn-1-yl)malonate

: 1434515-17-9
6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: lithium aluminium tetrahydride / dichloromethane / 1.25 h / 0 - 20 °C / Inert atmosphere

2: triethylamine / N,N-dimethyl-formamide / 0 - 20 °C

3: lithium diisopropyl amide / tetrahydrofuran; n-heptane; ethylbenzene / 5.25 h / -78 - 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; n-heptane; dichloromethane; ethylbenzene; N,N-dimethyl-formamide;
DOI:10.1021/ol400292q

Reference yield:

: 1434515-07-7
2-(3-(2-chlorophenyl)allyl)-2-(prop-2-yn-1-yl)propane-1,3-diol

: 1434515-17-9
6,6-bis(((tert-butyldimethylsilyl)oxy)methyl)-9-(2-chlorophenyl)non-8-en-3-yn-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / N,N-dimethyl-formamide / 0 - 20 °C

2: lithium diisopropyl amide / tetrahydrofuran; n-heptane; ethylbenzene / 5.25 h / -78 - 20 °C / Inert atmosphere

With triethylamine; lithium diisopropyl amide; In tetrahydrofuran; n-heptane; ethylbenzene; N,N-dimethyl-formamide;
DOI:10.1021/ol400292q