2-(Butoxymethyl)furan

Base Information

• Chemical Name: 2-(Butoxymethyl)furan
• CAS No.: 56920-82-2
• Molecular Formula: C9H14O2
• Molecular Weight: 154.209
• DSSTox Substance ID: DTXSID40205471
• Nikkaji Number: J75.465J
• Wikidata: Q83079057
• Mol file: 56920-82-2.mol

Synonyms:2-(Butoxymethyl)furan;56920-82-2;FURAN, 2-(BUTOXYMETHYL)-;2-butoxymethylfuran;BRN 0112762;MFCD01726117;2-17-00-00114 (Beilstein Handbook Reference);butyl furfuryl ether;2-butoxymethyl-furan;SCHEMBL1287680;DTXSID40205471;BBL103489;GEO-03142;STL557299;AKOS025212134;SB61209;s11931;LS-70074;MS-20638;A852928

Chemical Property of 2-(Butoxymethyl)furan

Chemical Property:

• Vapor Pressure: 1.07mmHg at 25°C
• Refractive Index: 1.4522 (estimate)
• Boiling Point: 183.1°Cat760mmHg
• Flash Point: 74.6°C
• PSA: 22.37000
• Density: 0.958g/cm³
• LogP: 2.59630
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 154.099379685
• Heavy Atom Count: 11
• Complexity: 93.6

Purity/Quality:

99%min ^*data from raw suppliers

2-(Butoxymethyl)furan ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCOCC1=CC=CO1

Technology Process of 2-(Butoxymethyl)furan

There total 8 articles about 2-(Butoxymethyl)furan 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: 82.4%

(2-furyl)methyl alcohol (98-00-0,25212-86-6,93793-62-5) + butan-1-ol (71-36-3) → furfuryl alcohol butyl ether (56920-82-2) + butyl levulinate (2052-15-5)

Guidance literature:

With carbonaceous glucose material functionalized with SO₃H; at 120 ℃; for 4h; Reagent/catalyst; Inert atmosphere;

DOI:10.1016/j.catcom.2019.02.016

Reference yield: 56.0%

(2-furyl)methyl alcohol (98-00-0,25212-86-6,93793-62-5) + butan-1-ol (71-36-3) → furfuryl alcohol butyl ether (56920-82-2) + dibutyl ether (142-96-1) + butyl levulinate (2052-15-5) + 5,5-dibutoxy-2-pentanone

Guidance literature:

With AQUIVION P₈₇S perfluorosulfonic acid resin; at 120 ℃; for 2h; Reagent/catalyst; Catalytic behavior; Sealed tube;

DOI:10.1039/c9nj03747k

Reference yield: 10.0%

2-furancarboxaldehyde dibutyl acetal (1829-09-0) → furfural (98-01-1) + furfuryl alcohol butyl ether (56920-82-2) + furan-2-carboxylic acid butyl ester (583-33-5)

Guidance literature:

With boron trifluoride diethyl etherate; In 1,2-dichloro-ethane; at 0 ℃; for 0.25h;

upstream raw materials:

2-furancarboxaldehyde dibutyl acetal

furfural

butan-1-ol

(2-furyl)methyl alcohol

Downstream raw materials:

butyl levulinate

Refernces

• 1、 Yang, Jinfan,Zhang, Hongyu,Ao, Zhifeng,Zhang, Sufeng. "Hydrothermal carbon enriched with sulfonic and carboxyl groups as an efficient solid acid catalyst for butanolysis of furfuryl alcohol". . p. 109 - 113. Retrieved 2019/07/02.
• 2、 Siva Sankar, Enumula,Saidulu Reddy,Jyothi, Yadagiri,David Raju, Burri,Rama Rao, Kamaraju Seetha. "Alcoholysis of Furfuryl Alcohol into n-Butyl Levulinate Over SBA-16 Supported Heteropoly Acid Catalyst". . p. 2807 - 2816. Retrieved 2017/09/14.