1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

Base Information

Chemical Name:1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol
CAS No.:678142-81-9
Molecular Formula:C₄₀H₆₈O₁₀Si₃
Molecular Weight:793.23
Hs Code.:

Synonyms:1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

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Technology Process of 1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

There total 6 articles about 1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol 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: 42.0%

: 994-30-9
triethylsilyl chloride

: DL-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-myo-inositol

: 678142-81-9
1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

: 204253-96-3
1D-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In chloroform; for 2h; Ambient temperature;
DOI:10.1016/S0040-4020(99)00551-7

Reference yield: 36.0%

: 994-30-9
triethylsilyl chloride

: 678142-80-8
D-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyl-disiloxane-1,3-diyl)-6-O-[(S)-O-acetylmandeloyl]-myo-inositol

: 678142-81-9
1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

: 204253-96-3
1D-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine;
DOI:10.1016/S0040-4039(98)00034-3

Reference yield:

: 51019-44-4
(S)-2-chloro-2-oxo-1-phenylethyl acetate

: 678142-81-9
1L-6-O-<(S)-(+)-O-acetylmandeloyl>-1,2-O-cyclohexylidene-3,4-O-(tetraisopropyldisiloxane-1,3-diyl)-5-O-triethylsilyl-myo-inositol

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / pyridine / CH₂Cl₂ / 16 h / 20 °C

2: ethyldiisopropylamine; DMAP / CH₂Cl₂ / 20 h / 20 °C

With pyridine; dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1002/ejoc.200300517