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

Base Information

Chemical Name:(S)-4-(3-Iodo-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester
CAS No.:761433-73-2
Molecular Formula:C₂₁H₂₄INO₄
Molecular Weight:481.33
Hs Code.:

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

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

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

There total 5 articles about (S)-4-(3-Iodo-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: 77.0%

: 137960-07-7
(S)-4-(4-Methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

: 761433-73-2
(S)-4-(3-Iodo-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Guidance literature:: With iodine; silver trifluoroacetate; In chloroform; at 25 ℃; for 4h;
DOI:10.1021/ja040090y

Reference yield:

: 13512-31-7
N-(benzyloxycarbonyl)-L-tyrosine methyl ester

: 761433-73-2
(S)-4-(3-Iodo-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / LiBH₄ / tetrahydrofuran / 2 h / 25 °C

2: 97 percent / p-toluenesulfonic acid / acetone / 0.5 h / 25 °C

3: 92 percent / K₂CO₃ / dimethylformamide / 10 h / 25 °C

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

With lithium borohydride; iodine; silver trifluoroacetate; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja040090y

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 761433-73-2
(S)-4-(3-Iodo-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / aq. Na₂CO₃ / CHCl₃ / 3 h / 25 °C

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

3: 97 percent / p-toluenesulfonic acid / acetone / 0.5 h / 25 °C

4: 92 percent / K₂CO₃ / dimethylformamide / 10 h / 25 °C

5: 77 percent / silver trifluoroacetate; I₂ / CHCl₃ / 4 h / 25 °C

With lithium borohydride; iodine; silver trifluoroacetate; sodium carbonate; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja040090y