(R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid

Base Information

• Chemical Name: (R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid
• CAS No.: 1333379-80-8
• Molecular Formula: C₁₇H₂₄O₅
• Molecular Weight: 308.375
• Mol file: 1333379-80-8.mol

Synonyms:(R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid

Chemical Property of (R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid

There total 2 articles about (R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid 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:

tert-butyl (R)-3-((S)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-5-benzyloxy-pentanoate (1181215-55-3) → (R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid (1333379-80-8)

Guidance literature:

tert-butyl (R)-3-((S)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-5-benzyloxy-pentanoate; With lithium hydrochloride monohydrate; dihydrogen peroxide; In tetrahydrofuran; water; at 0 - 20 ℃;

With hydrogenchloride; In tetrahydrofuran; water; pH=5;

Reference yield:

bromoacetic acid tert-butyl ester (5292-43-3) → (R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid (1333379-80-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / -78 - 20 °C

1.2: 20 °C

2.1: dihydrogen peroxide; lithium hydrochloride monohydrate / water; tetrahydrofuran / 0 - 20 °C

2.2: pH 5

With lithium hydrochloride monohydrate; dihydrogen peroxide; lithium hexamethyldisilazane; In tetrahydrofuran; water;

Reference yield:

(R)-2-(2-(benzyloxy)ethyl)-4-tert-butoxy-4-oxobutanoic acid (1333379-80-8) + methyl iodide (74-88-4) → (R)-4-tert-butyl 1-methyl 2-(2-(benzyloxy)ethyl)succinate (1333379-81-9)

Guidance literature:

With sodium hydrogencarbonate; In ISOPROPYLAMIDE; at 20 ℃;

upstream raw materials:

bromoacetic acid tert-butyl ester

tert-butyl (R)-3-((S)-4-benzyl-2-oxo-oxazolidine-3-carbonyl)-5-benzyloxy-pentanoate

Downstream raw materials:

(R)-4-tert-butyl 1-methyl 2-(2-(benzyloxy)ethyl)succinate

(R)-5-(benzyloxy)-3-(5-(triisopropylsilyloxy)-1H-indol-2-yl)pentanoic acid

(R)-methyl 5-(benzyloxy)-3-(5-(triisopropylsilyloxy)-1H-indol-2-yl)pentanoate

C₃₈H₅₉NO₇Si