HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700869Generated: October 31, 2026
3-(cyclopentyloxy)benzaldehyde → HCID 15453531, compound
https://huagongshe.com/reaction/1700869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(cyclopentyloxy)benzaldehyde | HCID 819981 | — |
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | HCID 15453530 | HCID 15453530 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15453531 | HCID 15453531 | — |
Reaction Steps
0.5 g of 2-(2-isopropoxyphenoxy)ethylamine (2.56 mmol) and 0.49 [lacuna] of 3-cyclopentyloxybenzaldehyde (2.56 mmol) are mixed together in 20 ml of toluene. The solution is refluxed for 12 hours, while continuously removing the water formed. The toluene is then evaporated off, the residue is taken up in 20 ml of methanol and the solution is cooled to 0° C. 0.28 g of potassium borohydride (5.12 mmol) is added portionwise and the mixture is stirred for 3 hours at room temperature. The methanol is evaporated off, the residue is taken up in dichloromethane and the organic phase is washed with water and then with saturated aqueous sodium chloride solution. The organic phase is dried over magnesium sulfate and filtered, and the solvent is evaporated off under vacuum. The title product is isolated by chromatography on a column of silica (eluent: 98/1.5/0.5 dichloromethane/methanol/aqueous ammonia). 0.77 g of the title product is obtained in the form of a pale yellow oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350913B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-ca0642067e2d47d3a47e8ed7f0abf932 |
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| Source note | uspto-grants-2002_02 |
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