(2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde

Base Information

Chemical Name:(2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde
CAS No.:478944-95-5
Molecular Formula:C₁₉H₂₇NO₃
Molecular Weight:317.428
Hs Code.:

Synonyms:(2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde

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Chemical Property of (2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde

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Technology Process of (2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde

There total 3 articles about (2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde 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: 65.0%

: 100-39-0
benzyl bromide

: 478944-86-4
(2R,4R)-4-Allyl-2-tert-butyl-4-hydroxymethyl-oxazolidine-3-carbaldehyde

: 478944-95-5
(2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; Heating;
DOI:10.1016/S0040-4039(02)01295-9

Reference yield:

: 93250-91-0,131233-89-1
(2R,4S)-2-tert-butyl-3-formyl-1,3-oxazolidine-4-carboxylic acid methyl ester

: 478944-95-5
(2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / LDA; HMPA / tetrahydrofuran / -78 - 0 °C

2: 75 percent / super-hydride / tetrahydrofuran / -78 °C

3: 65 percent / NaH; n-Bu₄NI / tetrahydrofuran / Heating

With N,N,N,N,N,N-hexamethylphosphoric triamide; tetra-(n-butyl)ammonium iodide; sodium hydride; lithium triethylborohydride; lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1016/S0040-4039(02)01295-9

Reference yield:

: 93250-96-5
(2R,4S)-methyl 4-allyl-2-tert-butyl-3-formyloxazolidine-4-carboxylate

: 478944-95-5
(2R,4R)-4-Allyl-4-benzyloxymethyl-2-tert-butyl-oxazolidine-3-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / super-hydride / tetrahydrofuran / -78 °C

2: 65 percent / NaH; n-Bu₄NI / tetrahydrofuran / Heating

With tetra-(n-butyl)ammonium iodide; sodium hydride; lithium triethylborohydride; In tetrahydrofuran;
DOI:10.1016/S0040-4039(02)01295-9