tert-Butyl nitrite
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3D model (JSmol)
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| ChemSpider | |||
| ECHA InfoCard | 100.007.962 | ||
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |||
| C4H9NO2 | |||
| Molar mass | 103.121 g·mol−1 | ||
| Appearance | colorless liquid | ||
| Boiling point | 61–63 °C (142–145 °F; 334–336 K) | ||
| Hazards | |||
| GHS labelling:[1] | |||
 
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| Danger | |||
| H225, H302, H332 | |||
| P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P301+P312, P303+P361+P353, P304+P312, P304+P340, P312, P330, P370+P378, P403+P235, P501 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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tert-Butyl nitrite is an organic compound with the formula (CH3)3CONO. A colorless liquid, it is the tert-butyl ester of nitrous acid and is typically employed as a solution with tert-butyl alcohol.
Use
[edit]The compound is used as a reagent in organic synthesis.[2] It reacts with secondary amides to give N-nitroso amides:[3]
- RC(O)N(H)R + (CH3)3CONO → RC(O)N(NO)R + (CH3)3COH
See also
[edit]References
[edit]- ^ "tert-Butyl nitrite". pubchem.ncbi.nlm.nih.gov. Retrieved 2 February 2022.
- ^ Di Qiu, He Meng, Liang Jin, Shengbo Tang, Shuai Wang, Fangyang Mo, Yan Zhang, Jianbo Wang (2014). "Synthesis of Arylboronic Pinacol Esters from Corresponding Arylamines". Organic Syntheses. 91: 106. doi:10.15227/orgsyn.091.0106.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Yedage, Subhash L.; Bhanage, Bhalchandra M. (2017). "Tert-Butyl Nitrite-Mediated Synthesis of N-Nitrosoamides, Carboxylic Acids, Benzocoumarins, and Isocoumarins from Amides". The Journal of Organic Chemistry. 82 (11): 5769–5781. doi:10.1021/acs.joc.7b00570. PMID 28472882.