(3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one

Base Information

Chemical Name:(3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one
CAS No.:220077-38-3
Molecular Formula:C₂₄H₂₉NO₆
Molecular Weight:428.486
Hs Code.:

Synonyms:(3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one

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Chemical Property of (3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one

Chemical Property:

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MSDS Files:: SDS file from LookChem

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Technology Process of (3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one

There total 3 articles about (3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-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: 50.0%

: 220077-26-9
1-[¹³C]-bromomethyl-4-(methoxymethyloxy)benzene

: 220077-24-7
(S)-2,3,5,6-tetrahydro-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazine-2-one

: 220077-38-3
(3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one

Guidance literature:: With sodium hexamethyldisilazane; In tetrahydrofuran; 1,2-dimethoxyethane; at -78 ℃; for 7h;
DOI:10.1016/S0040-4020(98)00995-8

Reference yield:

: 220077-36-1
Methylparaben-¹³C

: 220077-38-3
(3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / NaH / tetrahydrofuran / 0.33 h / 0 °C

2: 94 percent / LiAlH₄ / tetrahydrofuran / 1.5 h / 0 °C

3: 91 percent / LiBr, CH₃SO₂Cl, Et₃N / tetrahydrofuran / 1.5 h / -60 - 0 °C

4: 50 percent / sodium bis(trimethylsily)amide / tetrahydrofuran; 1,2-dimethoxy-ethane / 7 h / -78 °C

With lithium aluminium tetrahydride; sodium hexamethyldisilazane; sodium hydride; methanesulfonyl chloride; triethylamine; lithium bromide; In tetrahydrofuran; 1,2-dimethoxyethane;
DOI:10.1016/S0040-4020(98)00995-8

Reference yield:

: 220077-43-0
4-(methoxymethyloxy)phenyl[13C]methanol

: 220077-38-3
(3R,5S)-2,3,5,6-tetrahydro-3-[4-(methoxymethyloxy)phenyl[13C]methyl]-5-phenyl-N-(tert-butyloxycarbonyl)-4H-1,4-oxazin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / LiBr, CH₃SO₂Cl, Et₃N / tetrahydrofuran / 1.5 h / -60 - 0 °C

2: 50 percent / sodium bis(trimethylsily)amide / tetrahydrofuran; 1,2-dimethoxy-ethane / 7 h / -78 °C

With sodium hexamethyldisilazane; methanesulfonyl chloride; triethylamine; lithium bromide; In tetrahydrofuran; 1,2-dimethoxyethane;
DOI:10.1016/S0040-4020(98)00995-8