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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598622Generated: October 29, 2026

Triethylamine → (3-Azido-2-methylpropenyl)-benzene

https://huagongshe.com/reaction/598622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
Reactantalpha-Methylcinnamic alcoholHCID 6393846—
SolventDichloromethaneHCID 6344—
Product(3-Azido-2-methylpropenyl)-benzeneHCID 7663973389%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 100 mL round-bottomed flask equipped with a magnetic stir was added trans-2-methyl-3-phenyl-2-propen-1-ol (2.00 g, 13.5 mmol) and 75 mL of methylene chloride. The solution was then cooled to 0° C. while stirring. Then, triethylamine (2.75 g, 27.0 mmol) is added followed by a dropwise addition of methanesulfonyl chloride (2.34 g, 20.4 mmol) and a two hour stir period. The reaction mixture is washed with water (2×75 mL), dried with sodium sulfate and then concentrated de vacuo. The crude mixture is then dissolved in 75 mL of DMF and then stirred via magnetic stir bar. To this mixture, sodium azide (1.76 g, 27.0 mmol) is added. The reaction mixture is then heated to 80° C. and allowed to stir for two hours. At this time, volatiles are concentrated de vacuo and the resulting residue is purified via column chromatography (1:9 ethyl acetate/hexane) providing (3-Azido-2-methyl propenyl)-benzene (2.08 g, 89%) as a colorless oil. 1H NMR (300 MHz, CDCl3) δ 7.36-7.25 (m, 5H), δ 6.53 (s, 1H), δ 3.87 (s, 2H) ppm; 13C NMR (75 MHz, CDCl3) δ 129.4, 129.2, 128.9, 128.6, 128.4, 127.1, 59.9, 52.0, 22.3, 16.5 ppm; LRMS (EI) calcd for C10H11N3 (M+) 173. found 173.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897631B2
Source datasetuspto-grants-2011_03
ORD IDord-9baa4607597f489493c39904b35faf3e
Source noteuspto-grants-2011_03