HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396213Generated: November 1, 2026
Ethyl bromodifluoroacetate → HCID 71143765, compound
https://huagongshe.com/reaction/1396213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | 2-Bromo-5-fluoropyridine | HCID 2783171 | — |
| Reactant | HCID 71142816 | HCID 71142816 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 71143765 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901121B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-7703e03260e34c219132ccd0bcc505d1 |
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| Source note | uspto-grants-2014_12 |
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