(R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one

Base Information

Chemical Name:(R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one
CAS No.:185903-63-3
Molecular Formula:C₁₉H₂₅NO₄
Molecular Weight:331.412
Hs Code.:

Synonyms:(R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one

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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 (R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one

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Technology Process of (R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one

There total 1 articles about (R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-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: 99.0%

: 3973-43-1
4-methylpent-4-enal

: 101711-78-8,131685-53-5
(3R)-3-propionyl-4-benzyloxazolidin-2-one

: 185903-63-3
(R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one

Guidance literature:: With di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at -78 ℃;
DOI:10.1016/S0040-4039(96)02191-0

Reference yield:

: 185903-63-3
(R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one

: 185903-68-8
(2R,5S,6R)-2-Hydroxymethyl-2,6-dimethyl-5-(tetrahydro-pyran-2-yloxy)-cyclohexanone

Guidance literature:: Multi-step reaction with 6 steps

1: PPTS / CH₂Cl₂ / Heating

2: LiAlH₄ / tetrahydrofuran

3: Swern ox.

4: NH₂OH*HCl, AcONa / methanol / Ambient temperature

5: 88 percent / 7percent aq. NaOCl / CH₂Cl₂ / 8 h / Ambient temperature

6: 88 percent / H₂, B(OMe)3 / Raney Ni / H₂O; methanol / 1471.02 Torr / Ambient temperature

With sodium hypochlorite; lithium aluminium tetrahydride; Trimethyl borate; hydroxylamine hydrochloride; hydrogen; sodium acetate; pyridinium p-toluenesulfonate; nickel; In tetrahydrofuran; methanol; dichloromethane; water;
DOI:10.1016/S0040-4039(96)02191-0

Reference yield:

: 185903-63-3
(R)-4-Benzyl-3-((2R,3S)-3-hydroxy-2,6-dimethyl-hept-6-enoyl)-oxazolidin-2-one

: 185903-71-3
(2R,5S,6R)-2-(tert-Butyl-dimethyl-silanyloxymethyl)-2,6-dimethyl-5-(tetrahydro-pyran-2-yloxy)-cyclohexanone

Guidance literature:: Multi-step reaction with 7 steps

1: PPTS / CH₂Cl₂ / Heating

2: LiAlH₄ / tetrahydrofuran

3: Swern ox.

4: NH₂OH*HCl, AcONa / methanol / Ambient temperature

5: 88 percent / 7percent aq. NaOCl / CH₂Cl₂ / 8 h / Ambient temperature

6: 88 percent / H₂, B(OMe)3 / Raney Ni / H₂O; methanol / 1471.02 Torr / Ambient temperature

7: 97 percent / imidazole / dimethylformamide / Ambient temperature

With 1H-imidazole; sodium hypochlorite; lithium aluminium tetrahydride; Trimethyl borate; hydroxylamine hydrochloride; hydrogen; sodium acetate; pyridinium p-toluenesulfonate; nickel; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(96)02191-0