HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085283Generated: October 30, 2026
1,3-Dibromopropane → HCID 20061406, compound
https://huagongshe.com/reaction/1085283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dichloro-4-nitrophenol | HCID 12066 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 20061406 | HCID 20061406 | 94.8% |
Reaction Steps
A mixture of 4.16 g of 2,6-dichloro-4-nitrophenol, 40.4 g of 1,3-dibromopropane, 2.76 g of potassium carbonate and 2.46 g of potassium t-butoxide was heated under reflux for 4 hours in 50 ml of methyl ethyl ketone. The reaction mixture was allowed to cool down and insoluble matters were filtered off. The filtrate was concentrated under reduced pressure. The residue was dissolved in chloroform. The thus-prepared chloroform solution was washed with water, and the chloroform was then distilled off. The residue was purified by chromatography on a silica gel column (eluent: chloroform/hexane=4/1, by volume) to obtain 6.24 g of 1-bromo-3-(2,6-dichloro-4-nitrophenyloxy)propane. This compound was employed in the next reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05008267 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-0d2a0a8c0bf840bba81e04ba67592408 |
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| Source note | uspto-grants-1991_04 |
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