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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756918Generated: October 28, 2026

Diethyl aminosulfur trifluoride → 2-Dodecyl-alpha-fluoro-alpha-phenyl-2H-tetrazole-5-acetic acid, ethyl ester

https://huagongshe.com/reaction/1756918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl aminosulfur trifluorideHCID 53748433—
Reactant2-dodecyl-alpha-hydroxy-alpha-phenyl-2H-tetrazole-5-acetic acid, ethyl esterHCID 86748283—
SolventDichloromethaneHCID 6344—
Product2-Dodecyl-alpha-fluoro-alpha-phenyl-2H-tetrazole-5-acetic acid, ethyl esterHCID 5866324866.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 2-dodecyl-α-hydroxy-α-phenyl-2H-tetrazole-5-acetic acid, ethyl ester (0.45 g, 1.08 mmole) in CH2Cl2 (2 mL) was added dropwise to a -78° C. solution of diethyl amino sulfur trifluoride (DAST, J. Org. Chem. 1975;(40):574:578, 0.15 mL, 1.1 mmole) in CH2Cl2 (1 mL) under dry nitrogen. The mixture was stirred for 60 minutes at -78° C. before the cooling bath was removed and the solution allowed to warm to room temperature, where it was stirred an additional 3 hours. The mixture was poured into ice water and extracted with ethyl acetate (2×100 mL). The combined ethyl acetate extracts were washed with brine (50 mL) and dried. Filtration and concentration produced an oil which was flash chromatographed (silica gel, 7:1 hexane-ethyl acetate) to afford 0.3 g (66%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441975
Source datasetuspto-grants-1995_08
ORD IDord-d455c4620db04ddf82e977e099887a54
Source noteuspto-grants-1995_08