Direct Synthesis of Organic Azides from Alcohols Using 2-Azido-1,3-dimethyl­imidazolinium Hexafluorophosphate

Mitsuru Kitamura; Tatsuya Koga; Masakazu Yano; Tatsuo Okauchi

doi:10.1055/s-0031-1290958

Synlett, Inhaltsverzeichnis

Synlett 2012; 23(9): 1335-1338
DOI: 10.1055/s-0031-1290958

letter

Direct Synthesis of Organic Azides from Alcohols Using 2-Azido-1,3-dimethylimidazolinium Hexafluorophosphate

Autoren

Mitsuru Kitamura*

Department of Applied Chemistry, Kyushu Institute of Technology, 1-1 Sensuicho, Tobata, Kitakyushu 804-8550, Japan, Fax: +81(93)8843304 eMail: kita@che.kyutech.ac.jp
Tatsuya Koga

Department of Applied Chemistry, Kyushu Institute of Technology, 1-1 Sensuicho, Tobata, Kitakyushu 804-8550, Japan, Fax: +81(93)8843304 eMail: kita@che.kyutech.ac.jp
Masakazu Yano

Department of Applied Chemistry, Kyushu Institute of Technology, 1-1 Sensuicho, Tobata, Kitakyushu 804-8550, Japan, Fax: +81(93)8843304 eMail: kita@che.kyutech.ac.jp
Tatsuo Okauchi

Department of Applied Chemistry, Kyushu Institute of Technology, 1-1 Sensuicho, Tobata, Kitakyushu 804-8550, Japan, Fax: +81(93)8843304 eMail: kita@che.kyutech.ac.jp

Abstract

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Abstract

Direct synthesis of organic azides from alcohols was developed. Azide transfer of 2-azido-1,3-dimethylimidazolinium hexafluorophosphate (ADMP) to alcohols proceeds to give the corresponding azides under mild reaction conditions, which were easily isolated because the byproducts are highly soluble in water.

Key words

ADMP - azides - diazo compounds - azide transfer - heterocycles

Volltext

Referenzen

References and Notes

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9 ADMP (1) is a crystalline diazo transfer reagent having high thermal stability and low explosibility[8d,f] and is now commercially available from TCI (cat. No. A2457)
10 Typical Procedure for the Synthesis of Organic Azides from Alcohols with ADMP (1; Table 1, Entry 6) To a solution of 4-phenylbenzyl alcohol (2a, 185 mg, 1.0 mmol) in THF (5 mL), 2-azide-1,3-dimethylimidazolinium hexafluorophosphate (1, 332 mg, 1.2 mmol), and DBU (0.15 mL, 1.3 mmol) were added at r.t., and the mixture was stirred for 10 min. The reaction was quenched with sat. aq NH₄Cl, and organic materials were extracted with CH₂Cl₂. The combined extracts were washed with brine, and then dried over anhyd Na₂SO₄. The solvent was removed in vacuo to afford the crude compounds that were purified by flash column chromatography (silica gel, hexane–EtOAc) to give pure 4-biphenylmethylazide (3a) in 93% yield as a white solid. Physical Data for 3a Mp 35–36 °C. ¹H NMR (400 MHz, CDCl₃): δ = 7.62–7.57 (m, 4 H), 7.48–7.42 (m, 2 H), 7.42–7.32 (m, 3 H), 4.36 (s, 2 H) ppm. ¹³C NMR (101 MHz, CDCl₃): δ = 141.3, 140.5, 134.4, 128.9, 128.7, 127.6, 127.5, 127.1, 54.5 ppm. IR (Nujol): 2098, 1463, 1253, 823 cm^–1. Anal. Calcd for C₁₃H₁₁N₃: C, 74.62; H, 5.30; N, 20.08. Found: C, 74.76; H, 5.42; N, 19.99

Direct Synthesis of Organic Azides from Alcohols Using 2-Azido-1,3-dimethyl­imidazolinium Hexafluorophosphate

Autoren

Direct Synthesis of Organic Azides from Alcohols Using 2-Azido-1,3-dimethylimidazolinium Hexafluorophosphate