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HRID 1427829Erstellt: 26. Oktober 2026

Trichloroacetonitrile → 4-Bromo-2-chloro-5-fluorobenzyl 2,2,2-trichloroacetimidate

https://huagongshe.com/reaction/1427829

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrichloroacetonitrileHCID 11011—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt(4-Bromo-2-chloro-5-fluorophenyl)methanolHCID 67450751—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-2-chloro-5-fluorobenzyl 2,2,2-trichloroacetimidateHCID 8670285391,6%

Reaktionsschritte

To a solution of (4-bromo-2-chloro-5-fluorophenyl)methanol (3.95 g, 16.49 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (0.5 mL, 3.34 mmol) in methylene chloride (30 mL) was added trichloroacetonitrile (, 2.50 mL, 24.93 mmol) over 5 min at 0° C., stirring was continued for 4 h at 0° C. After concentrated in vacuo, the residue was purified by column chromatography eluting with 5% ethyl acetate in hexanes to give 4-bromo-2-chloro-5-fluorobenzyl 2,2,2-trichloroacetimidate as a colorless solid (5.80 g, 91%): δ 8.49 (s, 1H), 7.59 (d, J=6.3 Hz, 1H), 7.32 (d, J=9.0 Hz, 1H), 5.37 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08933236B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-453fe45170e24d2b92b44d91ffe2c6a6
Quellennotizuspto-grants-2015_01