HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752589Generated: October 28, 2026
Ethyl bromodifluoroacetate → Ethyl α,α-difluoro-2-quinolineacetate
https://huagongshe.com/reaction/1752589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Reactant | 2-Bromoquinoline | HCID 2762756 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl α,α-difluoro-2-quinolineacetate | HCID 10514875 | 70% |
Reaction Steps
A mixture of 2-bromoquinoline (5.0 g, 24.0 mmol), ethyl 2-bromo-2,2-difluoroacetate (5.8 g, 28.8 mmol) and copper power (3.5 g, 55.2 mmol) in DMSO (20 ml) was stirred at 55° C. for 5 hours. The solid was filtered off and water (100 ml) and EA (150 ml) were added. The organic layer was separated and evaporated and concentrated to give the title product (4.2 g, 70%) which was used for the next step without further purification. LC-MS (ESI+): m/e 252 (M+H)+, Rt: 0.934 min/2.5 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163019B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-e223211909e94354839bd2530332c1cd |
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| Source note | uspto-grants-2015_10 |
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