(R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one

Base Information

Chemical Name:(R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one
CAS No.:887602-34-8
Molecular Formula:C₂₅H₃₅NO₄Si
Molecular Weight:441.643
Hs Code.:

Synonyms:(R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one

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Chemical Property of (R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one

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Technology Process of (R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one

There total 1 articles about (R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-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: 97.0%

: 321921-73-7
(4R,2'R,3'S)-4-benzyl-3-[3-hydroxy-2-methylpent-4-enoyl]-oxazolidin-2-one

: 717910-28-6
(propynyl)diisopropylbromosilane

: 887602-34-8
(R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃; for 1h;
DOI:10.1021/ja0609708

Reference yield:

: 887602-34-8
(R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one

: 887602-20-2
3-ethylidene-2,3-diisopropyl-5-[2-(4-methoxy-benzyloxy)-1-methyl-ethyl]-4-methyl[1,2]oxasilolane

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / LiBH₄ / tetrahydrofuran / 6 h / 0 °C

2: 82 percent / CSA / CH₂Cl₂ / -10 - 20 °C

3: 65 percent / Ti(i-PrO)3Cl; i-PrMgCl / diethyl ether / 6 h

With triisopropoxytitanium(IV) chloride; lithium borohydride; camphor-10-sulfonic acid; isopropylmagnesium chloride; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/ja0609708

Reference yield:

: 887602-34-8
(R)-4-Benzyl-3-[(2R,3S)-3-(diisopropyl-prop-1-ynyl-silanyloxy)-2-methyl-pent-4-enoyl]-oxazolidin-2-one

: 887602-19-9
diisopropyl-{1-[2-(4-methoxy-benzyloxy)-1-methyl-ethyl]-allyloxy}-prop-1-ynyl-silane

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / LiBH₄ / tetrahydrofuran / 6 h / 0 °C

2: 82 percent / CSA / CH₂Cl₂ / -10 - 20 °C

With lithium borohydride; camphor-10-sulfonic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja0609708