(1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol

Base Information

Chemical Name:(1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol
CAS No.:851592-17-1
Molecular Formula:C₂₄H₄₄O₃Si₂
Molecular Weight:436.783
Hs Code.:

Synonyms:(1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol

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Chemical Property of (1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol

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Technology Process of (1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol

There total 5 articles about (1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol 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:

: 851592-00-2
(2R,3R,4S)-1,2-di(tert-butyldimethylsilyloxy)-3,4-epoxy-6-phenylhexane

: 851592-17-1
(1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol

: 851592-16-0
(1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-2,3-di-tert-butyldimethylsilyloxy-propan-1-ol

Guidance literature:: With n-butyllithium; potassium tert-butylate; diisopropylamine; In tetrahydrofuran; at -50 ℃; for 16h;
DOI:10.1016/j.tet.2005.01.102

Reference yield:

: 851592-11-5
(3E)-(2S)-1-(tert-butyldimethylsilyloxy)-6-phenylhex-3-en-2-ol

: 851592-17-1
(1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 231 mg / m-CPBA / CH₂Cl₂ / 20 °C

2: imidazole / CH₂Cl₂ / 2 h / 20 °C

3: 24 mg / BuLi; diisopropylamine; potassium tert-butoxide / tetrahydrofuran / 16 h / -50 °C

With 1H-imidazole; n-butyllithium; potassium tert-butylate; diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tet.2005.01.102

Reference yield:

: 851592-12-6
trans-(2R)-1-(tert-butyldimethylsilyloxy)-3,4-epoxy-6-phenylhexan-2-ol

: 851592-17-1
(1R,2R,1'S,2'S)-1-(trans-2'-phenylcyclopropyl)-1,3-di-tert-butyldimethylsilyloxypropan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: imidazole / CH₂Cl₂ / 2 h / 20 °C

2: 24 mg / BuLi; diisopropylamine; potassium tert-butoxide / tetrahydrofuran / 16 h / -50 °C

With 1H-imidazole; n-butyllithium; potassium tert-butylate; diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tet.2005.01.102