5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester

Base Information

• Chemical Name: 5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester
• CAS No.: 187996-38-9
• Molecular Formula: C₁₇H₂₀O₅S
• Molecular Weight: 336.409
• Mol file: 187996-38-9.mol

Synonyms:5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester

Chemical Property of 5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester

There total 4 articles about 5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl 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:

2-(1-Methyl-3-phenylsulfanyl-prop-2-ynyl)-3-oxo-hexanoic acid methyl ester (199919-22-7) → 5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester (187996-38-9)

Guidance literature:

With benzyltrismethylammonium methoxide; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction; 1.) CH₂Cl₂; 2.) THF, 40 deg C, 12 h;

DOI:10.1016/S0040-4039(97)10183-6

Reference yield:

methyl 3-oxohexanoate (30414-54-1) → 5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester (187996-38-9)

Guidance literature:

Multi-step reaction with 3 steps

1: NaH / tetrahydrofuran

2: MCPBA / CH₂Cl₂

3: benzyltrimethylammonium metoxide / methanol / 14 h

With sodium hydride; benzyltrismethylammonium methoxide; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; methanol; dichloromethane;

DOI:10.1016/S0040-4039(97)00074-9

Reference yield:

4-(phenylthio)but-3-yn-2-ol (190840-85-8) → 5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-carboxylic acid methyl ester (187996-38-9)

Guidance literature:

Multi-step reaction with 4 steps

1: 69 percent / PPh₃, I₂, imidazole

2: NaH / tetrahydrofuran

3: MCPBA / CH₂Cl₂

4: benzyltrimethylammonium metoxide / methanol / 14 h

With 1H-imidazole; iodine; sodium hydride; benzyltrismethylammonium methoxide; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane;

DOI:10.1016/S0040-4039(97)00074-9

upstream raw materials:

2-(1-Methyl-3-phenylsulfanyl-prop-2-ynyl)-3-oxo-hexanoic acid methyl ester

methyl 3-oxohexanoate

4-(phenylthio)but-3-yn-2-ol

(3-Iodo-but-1-ynylsulfanyl)-benzene

Downstream raw materials:

N-(1-{2-[10-Benzenesulfonyl-10-(3,4-dimethyl-5-propyl-furan-2-yl)-decyl]-5,5-dimethyl-[1,3]dioxan-2-yl}-2-hydroxy-ethyl)-benzenesulfonamide

2-Benzenesulfonylmethyl-3,4-dimethyl-5-propyl-furan

(5-Benzenesulfonylmethyl-4-methyl-2-propyl-furan-3-yl)-methanol