(1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

Base Information

Chemical Name:(1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne
CAS No.:157723-30-3
Molecular Formula:C₄₂H₈₀O₄Si₃
Molecular Weight:733.351
Hs Code.:

Synonyms:(1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

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Chemical Property of (1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

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Technology Process of (1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

There total 1 articles about (1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne 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:

: 81506-41-4
(1R,3aR,7aR)-1-{(1R)-1,5-dimethyl-5-[(trimethylsilyl)oxy]hexyl}-7a-methyloctahydro-4H-inden-4-one

: 116506-67-3
TB

: 157723-30-3
(1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction; 1.) ether, hexane, 0 deg C, 1 h, 2.) ether, hexane, from 0 deg C to RT;

Reference yield:

: 157723-30-3
(1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

: (1S,3R)-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholesta-5(10),6,7-triene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-BuLi / 1.) ether, hexane, from - 78 deg C to RT, 2.) ether, hexane, from -78 deg C to RT

2: 75.5 percent / SmI₂, Pd(PPh₃)4 / tetrahydrofuran; propan-2-ol / 14 h

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; samarium diiodide; In tetrahydrofuran; isopropyl alcohol;

Reference yield:

: 98-88-4
benzoyl chloride

: 157723-30-3
(1S,3R,8S)-8-hydroxy-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

: 157723-31-4
(1S,3R,8S)-8-(benzoyloxy)-1,3-bis<(tert-butyldimethylsilyl)oxy>-25-<(trimethylsilyl)oxy>-9,10-secocholest-5(10)-en-6-yne

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction; 1.) ether, hexane, from - 78 deg C to RT, 2.) ether, hexane, from -78 deg C to RT;