(S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde

Base Information

• Chemical Name: (S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde
• CAS No.: 178421-63-1
• Molecular Formula: C₁₁H₁₁NO₃
• Molecular Weight: 205.213
• Mol file: 178421-63-1.mol

Synonyms:(S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde

Chemical Property of (S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde

There total 6 articles about (S)-3-Benzyl-2-oxo-oxazolidine-5-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:

(R)-2,3-di-O-isoproylideneglyceraldehyde N-benzylimine (131319-74-9) → (S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde (178421-63-1)

Guidance literature:

Multi-step reaction with 5 steps

1: NaBH₄ / methanol / 0.5 h / 0 °C

2: 80 percent / DMAP / CH₂Cl₂ / 24 h / Ambient temperature

3: 100 percent / p-TosOH*H₂O / methanol / 4 h / Heating

4: 76 percent / NaH / tetrahydrofuran / 2 h / Ambient temperature

5: 1.) oxalylchloride, 2.) triethylamine / 1.) CH₂Cl₂, DMSO, -70 deg C, 20 min, 2.) CH₂Cl₂, DMSO, from -70 to 0 deg C

With dmap; sodium tetrahydroborate; Chloro-oxo-acetic acid; sodium hydride; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane;

DOI:10.1016/0040-4020(96)00309-2

Reference yield:

N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine (148638-80-6) → (S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde (178421-63-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / NaH / tetrahydrofuran / 2 h / Ambient temperature

2: 1.) oxalylchloride, 2.) triethylamine / 1.) CH₂Cl₂, DMSO, -70 deg C, 20 min, 2.) CH₂Cl₂, DMSO, from -70 to 0 deg C

With Chloro-oxo-acetic acid; sodium hydride; triethylamine; In tetrahydrofuran;

DOI:10.1016/0040-4020(96)00309-2

Reference yield:

N-benzyl-N-amine (109208-40-4) → (S)-3-Benzyl-2-oxo-oxazolidine-5-carbaldehyde (178421-63-1)

Guidance literature:

Multi-step reaction with 4 steps

1: 80 percent / DMAP / CH₂Cl₂ / 24 h / Ambient temperature

2: 100 percent / p-TosOH*H₂O / methanol / 4 h / Heating

3: 76 percent / NaH / tetrahydrofuran / 2 h / Ambient temperature

4: 1.) oxalylchloride, 2.) triethylamine / 1.) CH₂Cl₂, DMSO, -70 deg C, 20 min, 2.) CH₂Cl₂, DMSO, from -70 to 0 deg C

With dmap; Chloro-oxo-acetic acid; sodium hydride; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; methanol; dichloromethane;

DOI:10.1016/0040-4020(96)00309-2

upstream raw materials:

(5S)-3-benzyl-5-hydroxymethyloxazolidin-2-one

(R)-2,3-di-O-isoproylideneglyceraldehyde N-benzylimine

N-benzyl-N-amine

N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine