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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30567Generated: October 25, 2026

(Diethylamino)sulfur trifluoride → 1-Bromo-3-(4-fluorobut-1-ynyl)benzene

https://huagongshe.com/reaction/30567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(3-Bromophenyl)but-3-yn-1-olHCID 21895442—
SolventDichloromethaneHCID 6344—
Product1-Bromo-3-(4-fluorobut-1-ynyl)benzeneHCID 5743587664%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1.5 gm (6.67 mmol) of 4-(3-bromophenyl)but-3-yn-1-ol in CH2Cl2 at 0° C. was treated with 2.0 mL (15.3 mmol) of DAST, stirred at 0° C. for 1 h, allowed to warm to room temperature for 1 h, poured into saturated sodium bicarbonate and extracted with EtOAc. The combined extracts were washed sequentially with water and brine, dried over Na2SO4 and concentrated under reduced pressure. Chromatography of the resultant concentrate on silica gel with a gradient of 0% to 24% EtOAc-hexanes gave 1-Bromo-3-(4-fluoro-but-1-ynyl)benzene as a volatile liquid, 0.96 gm (64% yield); 1H NMR (400 MHz, CDCl3) δ: 2.82 (dt, 2H, J=6.6, 19.8 Hz), 4.56 (dt, 2H, J=6.6,46.4 Hz), 7.14 (t, 2H, J=7.9 Hz), 7.31 (m, 1H), 7.41 (m, 1H), 7.55 (t, 1H, J=1.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423158B2
Source datasetuspto-grants-2008_09
ORD IDord-99ffb0a02dac4ab3ad52c77f7a062294
Source noteuspto-grants-2008_09