HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840323Generated: October 28, 2026
Hydrochloric Acid → HCID 22622484, compound
https://huagongshe.com/reaction/840323
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromosalicylaldehyde | HCID 72863 | — |
| Reactant | Bromomethylcyclopropane | HCID 81503 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22622484 | HCID 22622484 | 22.8% |
Reaction Steps
To 5-bromosalicylaldehyde (15.0 g, 74 mmol) in dimethylformamide was added anhydrous potassium carbonate (36.8 g, 266 mmol) and bromomethylcyclopropane (9 ml, 93 mmol) and the solution stirred at 50 ° C. for 60 hours. Propylamine (26.5 g, 450 mmol) was then added and the solution left to stir at ambient temperatures for 2 hours, after which diethyl ether (50 ml) and sodium borohydride (2.6 g, 68 mmol) were added and the solution left for another hour. 6 Normal hydrochloric acid (150 ml) was then added dropwise and the solution left to stir for 16 hours. Impurities were extracted with diethyl ether (200 ml×2), the solution basified with caustic liquor and the product then extracted into diethyl ether (250 ml). The organic layer was then dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo to give the title compound (4.8 g, 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06365603B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-73cef8114a534fd890eb1f8f27ce8fdb |
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| Source note | uspto-grants-2002_04 |
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