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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537643Generated: October 28, 2026

(Diethylamino)sulfur trifluoride → HCID 44475673, compound

https://huagongshe.com/reaction/537643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantO-(2-Azidoethyl)heptaethylene glycolHCID 10960238—
SolventDichloromethaneHCID 6344—
ProductHCID 44475673HCID 4447567324.4%

Reaction Conditions

Temperature-10 °C

Reaction Steps

23-Azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol (500 mg, 1.26 mmol) was dissolved in DCM (2 mL) and cooled to −10° C. DAST (482 μL, 3.78 mmol) was added in portions to the cooled solution and the resulting mixture was stirred at −10° C. for 30 minutes then allowed to warm to room temperature and stirred for additional 20 hours. The excess of DAST was quenched with methanol (5 mL) and the solvents were subsequently evaporated at the reduced pressure. The oily residue was dissolved in the water (3 mL) and the pH was adjusted to 5 using NaHCO3. The crude product was purified on semipreparative HPLC (System E) to yield 122 mg (24%) of 4 as a yellowish oil. 1H NMR (500 MHz, CDCl3): δ 3.39 (t, J=5.0 Hz, 2H), 3.65-3.68 (m, 26H), 3.75 (dt, J=4.2 Hz, 29.6 Hz, 2H), 4.56 (dt, J=4.0 Hz, 47.5 Hz, 2H); 13C NMR (125.7 MHz, CDCl3): δ 50.8, 70.1, 70.4, 70.5, 70.7-70.8, 70.9, 83.2 (d, J=169 Hz); 19F NMR (470.6 MHz, CDCl3): δ −225.9; MS ESI (m/z): [M+H]+ calcd. for C16H33FO7N3, 398.2. found 398.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865122B2
Source datasetuspto-grants-2014_10
ORD IDord-b69d82004fa44e2693eb817e8823f686
Source noteuspto-grants-2014_10