HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280155Generated: October 30, 2026
1,3-Dibromopropane → HCID 20137129, compound
https://huagongshe.com/reaction/280155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 13711140 | HCID 13711140 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Product | HCID 20137129 | HCID 20137129 | — |
Reaction Steps
Potassium hydroxide (53 g, 87%) is added over a period of 1 hour 15 min to a stirred suspension of 4-hydroxy-1-piperidinylindan (30 g), and tetrabutylammonium chloride (4.1 g) in 1,3-dibromopropane (140 ml) and the resulting mixture stirred at RT under nitrogen for two hours. The reaction mixture is partitioned between ice-water and ether and the aqueous layer separated and extracted with ether. The combined organic extracts are washed with water and ice cold 5% aqueous HCl forming a precipitate which is filtered and washed with ether. The acidic fraction is made strongly alkaline forming an oil precipitate which is extracted into ether. The combined ether layers are washed, dried over Na2SO4, filtered and concentrated in vacuo yielding the desired product as an oil which is used in the next step without further treatment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04588719 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-55af7c317fc44146994bf071eebe0327 |
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| Source note | uspto-grants-1986_05 |
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