HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221694Generated: October 26, 2026
Diisopropylamine → 1-(5-Bromo-2-fluorophenyl)ethanone
https://huagongshe.com/reaction/221694
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethyl difluoroacetate | HCID 9961 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Bromo-2-fluorophenyl)ethanone | HCID 22607476 | — |
Reaction Steps
A solution of 17.78 ml (126 mmol) diisopropyl amine in 375 ml THF was cooled to −78° C. A 1.6 M solution of BuLi in hexanes (79 ml, 126 mmol) was added drop wise. After 15 minutes 20 g of 4-bromo-1-fluoro benzene (114 mmol) was added dropwise while keeping the temperature below −60° C. After stirring for 2.5 h at −70° C. 13.22 ml ethyl difluoro acetate were added. The mixture was warmed to −40° C. and then quenched by pouring the mixture onto 1M HCl. The mixture was extracted with ligroine, dried with MgSO4.H2O, concentrated and purified by column chromatography (silica gel; hexane/5-15% TBME) to give the desired product as a yellow liquid. 1H-NMR (CDCl3, 360 MHz): 8.09 (dd, 1H), 7.82-7.77 (m, 1H), 7.17 (t, 1H), 6.45 (t, 1H, CHF2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207164B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-427b36c0e2654461a3c729ab0e4a21d4 |
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| Source note | uspto-grants-2012_06 |
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