HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903549Generated: October 28, 2026
p-Bromochlorobenzene → HCID 23336425, compound
https://huagongshe.com/reaction/903549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | HCID 731601 | HCID 731601 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23336425 | HCID 23336425 | 26.5% |
Reaction Steps
To a phenylmagnesium bromide solution prepared from 6.9 g of p-chlorophenyl bromide, 0.88 g of magnesium and 25 ml of dry diethyl ether was added dropwise a solution of 2.42 g of 10-methyl-2,3,5,10-tetrahydroimidazo[2,1-b]quinazoline-5-one in 30 ml of dry tetrahydrofuran with stirring and ice-cooling. The mixture was heated under reflux for 2 hours and then cooled. To the mixture were added dropwise 20 ml of water and stirring was continued for a while. The resulting mixture was extracted with hot chloroform and the insoluble material was filtered off and washed with hot chloroform. The chloroform layer was dried over anhydrous sodium sulfate and concentrated to dryness under reduced pressure. The residue was crystallized from ethanol and the crystals were further recrystallized from dimethylformamide to give 1.0 g of 5-(p-chlorophenyl)-5-hydroxy-10-methyl-2,3,5,10-tetrahydroimidazo[2,1-b]quinazoline as colorless needles, m.p. 207°-209° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04228167 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-fc07e85cd0424333aa0a951db1c5204b |
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| Source note | uspto-grants-1980_10 |
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