HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193642Generated: October 26, 2026
1-Bromo-3-chloropropane → Methyl 4-(3-chloropropoxy)benzoate
https://huagongshe.com/reaction/1193642
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178524487 | HCID 178524487 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 4-(3-chloropropoxy)benzoate | HCID 12389265 | 106.7% |
Reaction Steps
Ethyl, 4-hydroxybenzoate 83.1 g (0.50 mole), 107 ml (1.0 mole) of 1-bromo-3-chloropropane, and potassium carbonate (1.5 mole, 207.3 g) were mechanically stirred in 600 ml of refluxing acetone under nitrogen overnight. The potassium carbonate was removed by filtration, and the filtrate was evaporated under reduced pressure to give 122 g of a liquid. This liquid was dissolved in 250 ml of petroleum ether and with stirring and cooling in an ice/2-propanol bath. A white precipitate formed and was collected by filtration and washed with cold petroleum ether to yield 108 g of a solid. An additional 6 g of the product was obtained from the mother liquor. A small sample of the solid was dissolved in petroleum ether at room temperature. The solution was stirred and cooled in an ice bath. White crystals were collected by filtration, washed with cold petroleum ether and dried under vacuum at room temperature, m.p. 24°-25° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04810713 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-e679d3abd206479ab2286c7d06ba4102 |
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| Source note | uspto-grants-1989_03 |
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