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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390606Generated: November 2, 2026

Triethylene Glycol → 2-(2-(2-Azidoethoxy)ethoxy)ethanol

https://huagongshe.com/reaction/2390606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylene GlycolHCID 8172—
ReactantAzideHCID 33558—
Reactant8-Trifluoroacetamido-3,6-dioxa-1-octanolHCID 57757146—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(2-(2-Azidoethoxy)ethoxy)ethanolHCID 11008438—

Reaction Steps

8-Trifluoroacetamido-3,6-dioxa-1-octanol (1f: 8-azido-3,6-dioxa-1-octanol (Amvamzollo, P. H.; Sinay, P. Carbohydr. Res. 1986, 150, 199-212) (0.7 g, 4.0 mmol) was synthesized from triethylene glycol following the reported procedure (Bertozzi, C. R.; Bednarski, M. D. J. Org. Chem. 1991, 56, 4326-4329). The azide was combined with Pd/C (150 mg) in MeOH (8.0 mL) and stirred 12 h under H2 (1 atm). The suspension was filtered over celite, and the filtrate was concentrated to afford the amine (0.590 g, 4.0 mmol) in quantitative yields (Sato, H.; Hayashi, E.; Yamada, N.; Yatagai, M.; Takahara, Y. Bioconjugate Chem. 2001, 12, 701-710.). Following general procedure 1, 2-[2-(2-aminoethoxy)ethoxy]ethanol (0.590 g, 3.95 mmol) was combined with triethylamine (1.378 mL, 9.89 mmol) and trifluoroacetic anhydride (0.782 mL, 5.54 mmol) in MeOH (5 mL). Purification by silica gel chromatography (EtOAc) yielded 0.576 g (60%) of if as a white solid. 1H (300 MHz, CD3OD): δ 7.87 (br s, 1H), 3.73 (m, 2H), 3.68-3.60 (m, 10H), 3.55 (t, 2H, J=4.5 Hz), 3.32 (br s, 1H); 13C (75 mHz, CD3OD): δ 157.6 (q, J=36.6 Hz), 116.1 (q, J=286.1 Hz), 72.68, 70.35, 70.24, 68.90, 61.52, 39.84; ESI-MS calcd for C8H14F3NO4 [M−H]−: 244.0797. found 244.0795.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273778B2
Source datasetuspto-grants-2012_09
ORD IDord-df7bc11e06524988890127080f3e1f85
Source noteuspto-grants-2012_09