:Adiponitrile

Because of the industrial value of adiponitrile, many methods have been developed for its synthesis. Early industrial methods started from furfural and later by the chlorination of butadiene to give 1,4-dichloro-2-butene, which with sodium cyanide, converts to 3-hexenedinitrile, which in turn can be hydrogenated to adiponitrile:

:ClCH₂CH=CHCH₂Cl + 2 NaCN → NCCH₂CH=CHCH₂CN + 2 NaCl

:NCCH₂CH=CHCH₂CN + H₂ → NC(CH₂)₄CN

Adiponitrile has also been produced from adipic acid, by dehydration of the diamide, but this is rarely employed.

After patent application in 2004, the majority of adiponitrile is prepared by the nickel-catalysed hydrocyanation of butadiene, as discovered at DuPont, pioneered by William C. Drinkard. The net reaction is:

:CH₂=CHCH=CH₂ + 2 HCN → NC(CH₂)₄CN

544x544px

The process involves several stages, the first of which involves monohydrocyanation (the addition of one molecule of HCN), affording isomers of pentenenitriles as well as 2- and 3-methylbutenenitriles. These unsaturated nitriles are subsequently isomerized to the 3-and 4-pentenenitriles. In the final stage, these pentenenitriles are subjected to a second hydrocyanation to produce adiponitrile, the anti-Markovnikov product, as well as 2-methylglutaronitrile, a useful byproduct.

Another side reaction is the alkene metathesis of 3-pentenenitrile to yield dicyanobutenes, which are readily hydrogenated to adiponitrile as described above.

The other major industrial method involves hydrodimerization, starting from acrylonitrile:{{cite journal

|last1=Cardoso |first1=D. S. |last2=Šljukić |first2=B. |last3=Santos |first3=D. M. |last4=Sequeira |first4=C. A.

|publication-date=July 17, 2017

|title=Organic Electrosynthesis: From Laboratorial Practice to Industrial Applications

|journal=Organic Process Research & Development |year=2017 |volume=21 |issue=9 |pages=1213–1226

|doi=10.1021/acs.oprd.7b00004}}{{cite journal|doi=10.1149/1.2426086|title=Electrolytic Reductive Coupling|journal=Journal of the Electrochemical Society|volume=111|issue=2|pages=215|year=1964|last1=Baizer|first1=Manuel M.}}

:2 CH₂=CHCN + 2 e⁻ + 2 H⁺ → NCCH₂CH₂CH₂CH₂CN

Image:AdiponitrileSynthesis.png

The electrolytic coupling of acrylonitrile was discovered at Monsanto Company.

Almost all adiponitrile is hydrogenated to hexane-1,6-diamine for the production of nylon:Robert A. Smiley "Hexamethylenediamine" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. {{doi|10.1002/14356007.a12_629}}

:NC(CH₂)₄CN + 4 H₂ → H₂N(CH₂)₆NH₂

Like other nitriles, adiponitrile is susceptible to hydrolysis; however, the resulting adipic acid is less expensively prepared via other routes.

In 2018, there existed approximately 1.5 million metric tons of capacity.{{citation needed|date=January 2023}} The main producers of adiponitrile were:{{cite journal |last1=Alexander |first1=Tullo |title=The chemical industry is bracing for a nylon 6,6 shortage |website=cen.acs.org |date=7 Oct 2018 |volume=96 |issue=40 |url=https://cen.acs.org/materials/polymers/chemical-industry-bracing-nylon-66/96/i40 |access-date=2 March 2021}}{{cite web |title=Ascend Finalizes $175 Million ADN Project in Alabama {{!}} CHEManager |url=https://www.chemanager-online.com/en/news-opinions/headlines/ascend-finalizes-175-million-adn-project-alabama |website=www.chemanager-online.com |access-date=2 March 2021}}

• Ascend Performance Materials: Decatur, Alabama (US); 400 metric kilotons per year (kt/y), expanded to 580 kt/y by 2022
• Invista: Victoria, Texas and Orange, Texas, (US)
• Invista and BASF "Butachimie ADN plant": Chalampé (France); production to be increased from 100 kt/y in 2020 to 600 kt/y
• Asahi Kasei (Japan)

BASF closed the 128 kt/y ADN plant at Seal Sands in 2009.{{cite journal |last1=Gale |first1=Lindsay |title=End of the line for Seal Sands |journal=KHL Group |date=1 April 2009 |url=https://www.khl.com/news/End-of-the-line-for-Seal-Sands/1034117.article |access-date=28 April 2023 |language=en}}

In 2015, the Shandong Runxing New Material 100 kt/y plant suffered an explosion and was not reopened. In 2022, Invista plans to open a 300–400 kt/y plant in Shanghai.{{cite web |title=INVISTA China ADN project receives final construction permit |url=https://www.invista.com/News-Articles/INVISTA-China-ADN-project-receives-final-construct |website=invista.com |access-date=2 March 2021}}

The {{LD50}} (median lethal dose) of adiponitrile is 300 mg/kg for oral ingestion by rats.

In 1990, ACGIH adopted a time-weighted average Threshold Limit Value of 2ppm for work-related skin exposure.2009 TLVs and BEIs, American Conference of Governmental Industrial Hygienists, Signature Publications, page 11 of 254.

The NIOSH recommended skin exposure limit for a work-related time weighted average concentration is 4ppm (18 mg/m³).[https://www.cdc.gov/niosh/npg/npgd0015.html NIOSH Pocket Guide] NIOSH Publication 2005-149; September 2005

Adiponitrile is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.{{Cite journal | publisher = Government Printing Office | title = 40 C.F.R.: Appendix A to Part 355—The List of Extremely Hazardous Substances and Their Threshold Planning Quantities | url = http://edocket.access.gpo.gov/cfr_2008/julqtr/pdf/40cfr355AppA.pdf | edition = July 1, 2008 | access-date = October 29, 2011 | archive-url = https://web.archive.org/web/20120225051612/http://edocket.access.gpo.gov/cfr_2008/julqtr/pdf/40cfr355AppA.pdf | archive-date = February 25, 2012 | url-status = dead }}

{{Reflist}}

• {{ICSC|0211|02}}
• {{PGCH|0015}}
• [http://www.chemicalland21.com/specialtychem/perchem/ADIPONITRILE.htm www.chemicalland.com]
• [http://webbook.nist.gov/cgi/cbook.cgi?ID=111-69-3&Units=SI www.nist.gov]

Category:Alkanedinitriles