HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425952Generated: October 26, 2026
1,4-Dibromobenzene → 3-(4-Bromophenyl)oxetan-3-ol
https://huagongshe.com/reaction/1425952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Oxetanone | HCID 15024254 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Bromophenyl)oxetan-3-ol | HCID 58382379 | — |
Reaction Steps
n-Butyllithium (1.6 mol/L in hexanes, 1.33 mL) was added to a solution of 1,4-dibromobenzene (0.50 g) in tetrahydrofuran (5 mL) cooled to −78° C. The solution was stirred at this temperature for 30 min prior to the dropwise addition of 3-oxetanone (0.15 g) dissolved in tetrahydrofuran (2 mL). The solution was warmed in the cooling bath to room temperature overnight. Aqueous NH4Cl solution was then added and the resulting mixture was extracted with ethyl acetate. The combined extracts were dried (Na2SO4) and the solvent was evaporated. The residue was purified by HPLC on reversed phase (acetonitrile/water) to give the title compound. Yield: 0.19 g (39% of theory); Mass spectrum (ESI−): m/z=273/275 (Br) [M+HCOO]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933072B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-a8c570b7953745ed953006999c22ef02 |
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| Source note | uspto-grants-2015_01 |
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