HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210535Generated: November 1, 2026
Bromocyclopentane → 3-Cyclopentyloxy-4-methoxybenzaldehyde
https://huagongshe.com/reaction/2210535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Isovanillin | HCID 12127 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Cyclopentyloxy-4-methoxybenzaldehyde | HCID 2735893 | — |
Reaction Steps
To a magnetically-stirred solution of isovanillin (557 mmol, 85.0 g) in dry DMF (500 mL) at room temperature was added powdered K2CO3 (558 mmol, 77.1 g) in one portion followed by the dropwise addition of neat cyclopentyl bromide (614 mmol, 91.5 g; 65.9 mL). The resulting suspension was warmed to 60° C. and the reaction monitored by TLC until complete. Upon completion, the reaction mixture was cooled to room temperature and the DMF was removed in vacuo. The residue was partitioned between H2O and EtOAc, the aqueous phase extracted with EtOAc and the combined organic layers were washed with H2O. The organics were dried (Na2SO4) and concentrated in vacuo to afford the alkylated product (317 mmol, 70.1 g; 57%) as a viscous oil which was of sufficient purity to be used as such in subsequent transformation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05459151 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-2b301a8ac81f4312b8e519eac1b20d1e |
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| Source note | uspto-grants-1995_10 |
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