HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867645Generated: October 31, 2026
HCID 57691462, compound → HCID 57691453, compound
https://huagongshe.com/reaction/1867645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57691462 | HCID 57691462 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57691453 | HCID 57691453 | — |
Reaction Steps
To a solution of 1-(2-(1,3-dioxan-2-yl)phenyl)-2-(3,5-bis(trifluoromethyl)benzyloxy)ethanone (1.06 g, 2.36 mmol) in tetrahydrofuran (15 mL) at −78° C. was added vinylmagnesium bromide (1 M in tetrahydrofuran, 4.73 mL, 4.73 mmol). The reaction was allowed to warm to −60° C. in the Dewar flask before quenching with saturated ammonium chloride. The reaction was poured into diethyl ether, washed with water, then brine, dried over magnesium sulfate, and concentrated. Column chromatography (12%-->25% EtOAc/Hex) gave 810 mg (72%) as a colorless oil. Mass spec.: 499.30 (MNa)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07632861B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-777ffb0228f94f9c817da898707c44a1 |
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| Source note | uspto-grants-2009_12 |
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