HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 468560Generated: October 30, 2026
1,2-Dibromoethane → HCID 54764462, compound
https://huagongshe.com/reaction/468560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 86669853 | HCID 86669853 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54764462 | HCID 54764462 | — |
Reaction Steps
Magnesium (Mg) (1.26 g) was suspended in tetrahydrofuran (THF) (10 ml), and a drop of 1,2-dibromoethane was added thereto. To the resulting mixture, 2,4,5-trifluorobenzene bromide (0.55 g) was added dropwise slowly and then stirred for 30 min. 2,4,5-trifluorobenzene bromide (9.0 g) dissolved in THF (50 ml) was added slowly dropwise to the resulting mixture for 30 min and then stirred at room temperature for 1 hour. CuI (0.72 g) was added to the resulting mixture and the reaction temperature was cooled to 0° C. (S)-epichlorohydrin (4.1 ml) dissolved in THF (40 ml) was added dropwise to the resulting mixture slowly over 30 min, heated to room temperature, and stirred for 2 hours. Satuated NH4Cl (50 ml) and ethyl acetate (50 ml) were added to the resulting mixture, and the organic layer formed thereafter was separated. The separated organic layer was washed with 50 ml of satuated saline, dried over MgSO4, and filtered. The organic solvent was removed from the filtrate under a reduced pressure to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08624026B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-d279b29a4cec4792b2694db03f48b2b6 |
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| Source note | uspto-grants-2014_01 |
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