HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028954Generated: November 2, 2026
Lithium Chloride → (2-Bromophenyl)(tetrahydro-2H-pyran-4-yl)methanone
https://huagongshe.com/reaction/1028954
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Oxane-4-carbonyl chloride | HCID 2795505 | — |
| Reactant | Pentamethylene-1,5-bis(magnesium bromide) | HCID 3637391 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Reactant | HCID 178419606 | HCID 178419606 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Bromophenyl)(tetrahydro-2H-pyran-4-yl)methanone | HCID 63936269 | — |
Reaction Steps
Lithium chloride (0.16 mL, 7.8 mmol) and copper cyanide (0.12 mL, 3.9 mmol) were dissolved in dry THF (4 mL) under nitrogen. This was added dropwise to pentamethylenebis(magnesium bromide) (0.5 M in THF, 7.79 mL, 3.9 mmol) in a dry ice bath under nitrogen and the mixture stirred for 30 min. I-Bromo-2-iodobenzene (0.50 mL, 3.9 mmol) was added and the flask was removed from the cold bath. After 30 min additional dry THF (5 mL) was added and stirred for another 40 min. Then tetrahydro-2H-pyran-4-carbonyl chloride (0.58 mL, 3.9 mmol) was added in one portion, and the mixture was stirred for 15 min. The reaction was quenched by addition of saturated ammonium chloride (10 mL). Ethyl acetate (100 mL) and water (100 mL) were added and the phases were mixed and separated. The organic layer was separated, dried with magnesium sulfate and evaporated to dryness under reduced pressure. Purification using silica column chromatography (hexane to ethyl acetate gradient) gave (2-bromophenyl)(tetrahydro-2H-pyran-4-yl)methanone as a thick oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735384B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-dff836534f2b4667bc15b944c9965aa3 |
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| Source note | uspto-grants-2014_05 |
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