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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625499Generated: October 30, 2026

Sodium Azide → Benzyl 3-(1-azido-3,6,9,12-tetraoxapentadec-14-yn-15-yl)benzoate

https://huagongshe.com/reaction/625499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl 3-(1-(tosyloxy)-3,6,9,12-tetraoxapentadec-14-yn-15-yl)benzoateHCID 86705995—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzyl 3-(1-azido-3,6,9,12-tetraoxapentadec-14-yn-15-yl)benzoateHCID 86705994—

Reaction Conditions

Temperature80 °C

Reaction Steps

Into a 1000-mL round-bottom flask, was placed a solution of benzyl 3-(1-(tosyloxy)-3,6,9,12-tetraoxapentadec-14-yn-15-yl)benzoate (35.4 g, 59.30 mmol, 1.00 equiv) in N,N-dimethylformamide (400 mL), sodium bicarbonate (10 g, 119.05 mmol, 2.00 equiv), sodium azide (11 g, 169.23 mmol, 3.00 equiv). The resulting solution was stirred overnight at 80° C. The resulting solution was diluted with 200 mL of water. The resulting solution was extracted with 3×100 mL of ethyl acetate and the organic layers combined. The resulting mixture was washed with 3×100 mL of NaHCO3 aq. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 25 g (90%) of benzyl 3-(1-azido-3,6,9,12-tetraoxapentadec-14-yn-15-yl)benzoate as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301951B2
Source datasetuspto-grants-2016_04
ORD IDord-b9753572796b4807b63c29fe27023995
Source noteuspto-grants-2016_04