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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(3-Bromophenyl)but-3-yn-1-ol | HCID 21895442 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Bromo-3-(4-fluorobut-1-ynyl)benzene | HCID 57435876 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423158B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-99ffb0a02dac4ab3ad52c77f7a062294 |
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| Source note | uspto-grants-2008_09 |
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