(2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

Base Information

Chemical Name:(2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine
CAS No.:205440-44-4
Molecular Formula:C₂₉H₃₃NO₆
Molecular Weight:491.584
Hs Code.:

Synonyms:(2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

Suppliers and Price of (2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

There total 1 articles about (2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine 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: 91.4%

: 125261-01-0
2-(2-phenyl-1,3-dioxolan-2-yl)acetaldehyde

: 204845-22-7
(R)-N-2,4,6-trimethoxybenzylphenylglycinol

: 205440-44-4
(2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

Guidance literature:: With 3 A molecular sieve; In dichloromethane; for 18h; Ambient temperature;

Reference yield: 95.8%

: 62563-07-9
2-(3-bromopropyl)-1,3-dioxolane

: 205440-44-4
(2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

: 205440-45-5
(R)-2-[(S)-4-[1,3]Dioxolan-2-yl-1-(2-phenyl-[1,3]dioxolan-2-ylmethyl)-butylamino]-2-phenyl-ethanol

Guidance literature:: With magnesium; In tetrahydrofuran; at 0 ℃; for 48h;

Reference yield:

: 205440-44-4
(2R,4R)-N-(2,4,6-trimethoxybenzyl)-2-(2,2-ethylenedioxy-2-phenylethyl)-4-phenyl-1,3-oxazolidine

: 205440-52-4
(S)-N-ethoxycarbonyl-2-phenacylpiperidine

Guidance literature:: Multi-step reaction with 6 steps

1: 95.8 percent / magnesium / tetrahydrofuran / 48 h / 0 °C

2: 1 N hydrochloric acid / methanol / 2 h / Ambient temperature

3: sodium borohydride / methanol / 0.67 h / Ambient temperature

4: hydrogen / palladium hydroxide on carbon / methanol / 48 h / 2280 - 3040 Torr

5: diisopropylethylamine, 4-(dimethylamino)pyridine / CH₂Cl₂ / 4 h / Ambient temperature

6: 97.6 percent / 5percent hydrochloric acid / tetrahydrofuran / 18 h / Ambient temperature

With hydrogenchloride; dmap; sodium tetrahydroborate; hydrogen; magnesium; N-ethyl-N,N-diisopropylamine; palladium dihydroxide; In tetrahydrofuran; methanol; dichloromethane;