(S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Base Information

• Chemical Name: (S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester
• CAS No.: 761433-74-3
• Molecular Formula: C₃₀H₃₄BrNO₇
• Molecular Weight: 600.506
• Mol file: 761433-74-3.mol

Synonyms:(S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Chemical Property of (S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

There total 8 articles about (S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester 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: 69.0%

isopropylmagnesium bromide (920-39-8) + O-methoxymethyl-3-bromosalicylaldehyde (236094-18-1) + (S)-4-(3-Iodo-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester (761433-73-2) → (S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester (761433-74-3)

Guidance literature:

isopropylmagnesium bromide; (S)-4-(3-Iodo-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester; In tetrahydrofuran; at -20 ℃;

O-methoxymethyl-3-bromosalicylaldehyde; In tetrahydrofuran; at -78 ℃; for 0.166667h;

DOI:10.1021/ja040090y

Reference yield:

2,6-dibromophenol (608-33-3) → (S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester (761433-74-3)

Guidance literature:

Multi-step reaction with 3 steps

1.1: NaH / tetrahydrofuran / 0.08 h / 0 °C

1.2: 97 percent / tetrahydrofuran / 2 h / 25 °C

2.1: n-BuLi / tetrahydrofuran / 0.17 h / -78 °C

2.2: 67 percent / tetrahydrofuran / -78 - 25 °C

3.1: tetrahydrofuran / -20 °C

3.2: 69 percent / tetrahydrofuran / 0.17 h / -78 °C

With n-butyllithium; sodium hydride; In tetrahydrofuran; 3.2: Grignard reaction;

DOI:10.1021/ja040090y

Reference yield:

N-(benzyloxycarbonyl)-L-tyrosine methyl ester (13512-31-7) → (S)-4-{3-[(3-Bromo-2-methoxymethoxy-phenyl)-hydroxy-methyl]-4-methoxy-benzyl}-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester (761433-74-3)

Guidance literature:

Multi-step reaction with 5 steps

1.1: 99 percent / LiBH₄ / tetrahydrofuran / 2 h / 25 °C

2.1: 97 percent / p-toluenesulfonic acid / acetone / 0.5 h / 25 °C

3.1: 92 percent / K₂CO₃ / dimethylformamide / 10 h / 25 °C

4.1: 77 percent / silver trifluoroacetate; I₂ / CHCl₃ / 4 h / 25 °C

5.1: tetrahydrofuran / -20 °C

5.2: 69 percent / tetrahydrofuran / 0.17 h / -78 °C

With lithium borohydride; iodine; silver trifluoroacetate; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide; acetone; 5.2: Grignard reaction;

DOI:10.1021/ja040090y

upstream raw materials:

isopropylmagnesium bromide

O-methoxymethyl-3-bromosalicylaldehyde

(S)-4-(3-Iodo-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

2,6-dibromophenol

Downstream raw materials:

(S)-4-[3-(3-Bromo-2-methoxymethoxy-benzoyl)-4-methoxy-benzyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester