HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881771Generated: October 30, 2026
1,4-Dibromobenzene → HCID 86700876, compound
https://huagongshe.com/reaction/881771
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | 4-Methylenecyclohexanone | HCID 573489 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86700876 | HCID 86700876 | 36.7% |
Reaction Steps
To a flask charged with dry, freshly ground magnesium turnings (1.1 g, 45 mmol) and iodine (25 mg, 0.1 mmol) in THF (50 mL) was added a solution of 1,4-dibromobenzene (10.6 g, 45.0 mmol) in THF (30 mL) slowly by dropping funnel over 30 min. The resulting mixture was stirred at rt for 1 hr. The resultant grey Grignard solution was cooled to −78° C. and to it was added a solution of 4-methylenecyclohexanone (3.3 g, 30 mmol) in THF (20 mL) slowly dropwise over 20 min. The reaction was stirred at −78° C. for 30 min before being allowed to stir and warm to rt for 3 h. The resulting reaction mixture was quenched with a saturated aqueous NH4Cl solution and extracted with methyl tert-butyl ether. The combined organic phases were washed with a saturated aqueous NaCl solution, dried over MgSO4, filtered and concentrated by rotary evaporation in vacuo to afford a crude yellow oil. Purification of the crude material by column chromatography (80 g silica gel, 0-50% EtOAc:Hept, monitor for 225 nm) afforded 2.94 g of a colorless oil that was used without further purification. ESI-MS m/z: not ionized [M+H]+, retention time 1.50 min (condition E).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993619B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-e1d785dcd0bf4346bfd4f741ec5d4dce |
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| Source note | uspto-grants-2015_03 |
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