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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406612Generated: November 3, 2026

Ethyl bromodifluoroacetate → HCID 71143765, compound

https://huagongshe.com/reaction/2406612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromodifluoroacetateHCID 69585—
Reactant2-Bromo-5-fluoropyridineHCID 2783171—
ReactantHCID 71142816HCID 71142816—
CatalystCopperHCID 23978—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 71143765HCID 71143765—

Reaction Steps

Compound 10 was prepared in a similar manner to compound 1. To a stirred solution of ethyl 2-bromo-2,2-difluoroacetate (2.18 mL, 17.0 mmol) in DMSO (18 mL) was added copper powder (2.16 g, 34.0 mmol) at RT under N2 atmosphere. After being stirred for 2 h at RT, 2-bromo-5-fluoropyridine (1.50 g, 8.52 mmol) was then added, and stirring was continued for 3 h at RT. The progress of the reaction was monitored by TLC. The reaction was quenched with aqueous NH4Cl and extracted with CH2Cl2 (3×50 mL). The combined organic layers were washed with water and brine, dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford crude product mixture. Purification by column chromatography (eluting with EtOAc/hexane) afforded the ester (1.40 g, 6.3 mmol, 77%) as a pale yellow oil. 1H NMR (500 MHz, CDCl3): δ 8.50 (s, 1H), 7.78 (dd, J=9.0, 4.0 Hz, 1H), 7.60-7.51 (m, 1H), 4.42-4.32 (m, 2H), 1.39-1.31 (m, 3H). MS (ESI): m/z 220 [M++1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809378B2
Source datasetuspto-grants-2014_08
ORD IDord-f9365ca736c147899e02b62985c0b6b7
Source noteuspto-grants-2014_08