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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111520Generated: November 1, 2026

Sodium Azide → tert-Butyl 12-amino-4,7,10-trioxadodecanoate

https://huagongshe.com/reaction/2111520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantAzido-PEG3-t-butyl esterHCID 60146206—
Reactant3-{2-[2-(2-Tosylsulfonyloxy-ethoxy)-ethoxy]-ethoxy}-propionic acid tert-butyl esterHCID 86607621—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 12-amino-4,7,10-trioxadodecanoateHCID 16218573—

Reaction Steps

NaN3 (35 g, 538 mmol) was added to a stirring solution of 3-{2-[2-(2-tosylsulfonyloxy-ethoxy)-ethoxy]-ethoxy}-propionic acid tert-butyl ester (20 g, 46 mmol) in DMF (150 mL) and the reaction was stirred overnight. Reaction was diluted with water (200 mL) and extracted with EtOAc (4×100 mL). The organic layer was washed with water (100 mL) and brine (100 mL) and dried over Na2SO4. The solvent was removed in vacuo to give an oil. Column chromatography EtOAc/Hex (1:4) gave an oil which corresponds to the 3-{2-[2-(2-azido-ethoxy)-ethoxy]-ethoxy}-propionic acid tert-butyl ester, (M+1)=304. This oil was hydrogenated using Pd (5% on carbon) in EtOAc under hydrogen (1 atm.) over 3 days. The catalyst was removed by filtration and solvent removed in vacuo to give an oil corresponding to the title compound, (M+1)=278.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521425B2
Source datasetuspto-grants-2009_04
ORD IDord-f4a7efac56734fd4b1db9662d9ce00e5
Source noteuspto-grants-2009_04