HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706168Generated: November 2, 2026
1,3-Dibromopropane → HCID 13961622, compound
https://huagongshe.com/reaction/1706168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 20185710 | HCID 20185710 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13961622 | HCID 13961622 | 87.8% |
Reaction Steps
N-(p-methoxybenzyloxy)-p-toluenesulfonamide (61.4 g) was added to a solution of sodium ethoxide in absolute ethanol (Na: 4.6 g, absolute C2H5OH: 540 ml) and stirred at 70° C. for 1.5 hours. After cooling at ambient temperature, 1,3-dibromopropane (121.2 g) was added to the mixture, and then the mixture was refluxed with stirring for 2 hours and filtered. The filtrate was concentrated under reduced pressure. To the residue was added a mixture of ethyl acetate and water, and the organic layer was separated, dried over magnesium sulfate and evaporated to dryness under reduced pressure to give an oil, which was crystallized from a mixture of ethyl acetate and n-hexane to give N-(3-bromopropyl)-N-(p-methoxybenzyloxy)-p-toluenesulfonamide (75.1 g). MP: 89.5°-91.5° C. In substantially the same manner as described in the above example, there were obtained the following compounds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04206156 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-33844ed32b0840c6aaac1e07d1a8c6d6 |
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| Source note | uspto-grants-1980_06 |
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