(2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran

Base Information

• Chemical Name: (2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran
• CAS No.: 1449521-36-1
• Molecular Formula: C₁₃H₁₆FIO₂
• Molecular Weight: 350.172
• Mol file: 1449521-36-1.mol

Synonyms:(2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran

Chemical Property of (2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran

There total 4 articles about (2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran 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: 99.0%

(2S,5S)-5-[(4-fluorophenoxy)methyl]-2-[1′-hydroxyethyl]tetrahydrofuran (1449521-35-0) → (2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran (1449521-36-1)

Guidance literature:

With 1H-imidazole; iodine; triphenylphosphine; In tetrahydrofuran; at 0 ℃; for 4h;

DOI:10.1055/s-0033-1338934

Reference yield:

(2S,5S)-2-[2′-(tert-butyldiphenylsilyloxy)ethyl]-5-[(4-fluorophenoxy)methyl]tetrahydrofuran (1449521-34-9) → (2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran (1449521-36-1)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 h

2: triphenylphosphine; iodine; 1H-imidazole / tetrahydrofuran / 4 h / 0 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; iodine; triphenylphosphine; In tetrahydrofuran;

DOI:10.1055/s-0033-1338934

Reference yield:

C29H35FO4Si (1263497-40-0) → (2S,5S)-2-[(4-fluorophenoxy)methyl]-5-[2'-(iodoethyl)]tetrahydrofuran (1449521-36-1)

Guidance literature:

Multi-step reaction with 4 steps

1: tetrahydrofuran / 24 h / 70 °C

2: tri-n-butyl-tin hydride; 2,2'-azobis(isobutyronitrile) / toluene / 3 h / 120 °C

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 h

4: triphenylphosphine; iodine; 1H-imidazole / tetrahydrofuran / 4 h / 0 °C

With 1H-imidazole; 2,2'-azobis(isobutyronitrile); tetrabutyl ammonium fluoride; iodine; tri-n-butyl-tin hydride; triphenylphosphine; In tetrahydrofuran; toluene;

DOI:10.1055/s-0033-1338934

upstream raw materials:

C₂₉H₃₅FO₄Si

O-(2R,3R,5S)-2-[2'-(tert-butyldiphenylsilyloxy)ethyl]-5-[(p-fluorophenoxy)methyl]tetrahydrofuran-3-yl-1H-imidazole-1-carbothioate

(2S,5S)-2-[2′-(tert-butyldiphenylsilyloxy)ethyl]-5-[(4-fluorophenoxy)methyl]tetrahydrofuran

(2S,5S)-5-[(4-fluorophenoxy)methyl]-2-[1′-hydroxyethyl]tetrahydrofuran

Downstream raw materials:

(2S,5S)-2-[(4-fluorophenoxy)methyl]-5-vinyltetrahydrofuran

(2S,5S)-2-ethynyl-5-[(4-fluorophenoxy)methyl]tetrahydrofuran

C₁₂H₁₃FO₃