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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924210Generated: October 31, 2026

(Bis(2-methoxyethyl)amino)sulfur trifluoride → HCID 90405135, compound

https://huagongshe.com/reaction/924210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
ReactantHCID 90404401HCID 90404401—
SolventDichloromethaneHCID 6344—
ProductHCID 90405135HCID 9040513547%

Reaction Steps

To the crude ethyl 2-fluoro-3-hydroxy-3-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)phenyl)propanoate (0.11 g, 0.26 mmol) in dichloromethane (1.7 mL) at 0° C. was added Deoxo-Fluor® (0.05 mL, 0.28 mmol) and stirred for 30 minutes. The reaction mixture was loaded onto a Celite® cartridge and purified by flash column chromatography using 0-60% ethyl acetate/hexanes as eluent to afford the title compound as a yellow oil (0.054 g, 47%): 1H NMR (400 MHz, CDCl3) δ 8.58 (d, J=1.9 Hz, 1H), 8.32-8.14 (m, 2H), 7.87-7.73 (m, 2H), 7.50 (d, J=8.1 Hz, 2H), 7.39 (d, J=8.6 Hz, 2H), 6.11-5.76 (m, 1H), 5.52-4.90 (m, 1H), 4.27 (dqd, J=23.6, 7.1, 2.1 Hz, 2H), 1.27 (dt, J=19.4, 7.1 Hz, 3H); 19F NMR (376 MHz, CDCl3) δ −58.04, −187.64, −187.68, −192.41, −192.44, −202.56, −202.60, −204.97, −205.00; ESIMS m/z 442 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278964B2
Source datasetuspto-grants-2016_03
ORD IDord-a2ebaa9648b1472285e7dcbac14fa7eb
Source noteuspto-grants-2016_03