HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708463Generated: October 30, 2026
HCID 178418573, compound → HCID 178441842, compound
https://huagongshe.com/reaction/1708463
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Reactant | HCID 178441846 | HCID 178441846 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178441842 | HCID 178441842 | — |
Reaction Steps
To a solution of 4.00 g of 6-acetyl-2-butyl-4-(1H)-quinazolinone in 250 ml of dry tetrahydrofuran, cooled to 0° C., is added dropwise 16.4 ml of 3.0M methylmagnesium bromide in diethyl ether. The reaction is stirred at 0° C. for 0.5 hours and then allowed to warm to room temperature followed by quenching with 100 ml of saturated ammonium chloride solution. The mixture is diluted with 50 ml of water and extracted with ethyl acetate. The combined organic layers are washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue is purified by flash chromatography on silica gel, eluting with 100:0.25 chloroform-methanol to give 2.75 g of the desired product as a white solid. CI MASS SPEC 261(MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05358951 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-2d295615b4c740908dbdfefad218def2 |
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| Source note | uspto-grants-1994_10 |
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