(-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate

Base Information

Chemical Name:(-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate
CAS No.:391198-96-2
Molecular Formula:C₃₁H₄₈O₇
Molecular Weight:532.718
Hs Code.:

Synonyms:(-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate

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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 (-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate

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Technology Process of (-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate

There total 14 articles about (-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate 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: 100.0%

: 391198-95-1
(+)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-8'-O'-(tert-butyldimethylsilyl)bishomononactoyl]bishomononactate

: 391198-96-2
(-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate

Guidance literature:: With hydrogen fluoride; In acetonitrile;
DOI:10.1271/bbb.65.2118

Reference yield:

: 391198-93-9,17488-13-0
(-)-bishomononactic acid

: 391198-96-2
(-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate

Guidance literature:: Multi-step reaction with 5 steps

1.1: t-BuOK / dimethylformamide / 65 °C

2.1: imidazole / tetrahydrofuran

3.1: H₂ / 10 percent Pd/C / methanol

4.1: (PyS)2; PPh₃ / toluene / Heating

4.2: 86 percent / AgClO₄ / toluene

5.1: 100 percent / HF / acetonitrile

With 1H-imidazole; hydrogen fluoride; potassium tert-butylate; hydrogen; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1271/bbb.65.2118

Reference yield:

: (R)-2-[(2R,5S)-5-((R)-2-Hydroxy-3-methyl-butyl)-tetrahydro-furan-2-yl]-propionic acid benzyl ester

: 391198-96-2
(-)-benzyl (2S,3S,6R,8S)-8-O-[(2'R,3'R,6'S,8'R)-bishomononactoyl]bishomononactate

Guidance literature:: Multi-step reaction with 4 steps

1.1: imidazole / tetrahydrofuran

2.1: H₂ / 10 percent Pd/C / methanol

3.1: (PyS)2; PPh₃ / toluene / Heating

3.2: 86 percent / AgClO₄ / toluene

4.1: 100 percent / HF / acetonitrile

With 1H-imidazole; hydrogen fluoride; hydrogen; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; methanol; toluene; acetonitrile;
DOI:10.1271/bbb.65.2118