HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703526Generated: October 30, 2026
Water → 4-(2-(Pyrrolidin-1-yl)ethoxy)benzaldehyde
https://huagongshe.com/reaction/703526
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4-(2-Bromoethoxy)Benzaldehyde | HCID 262706 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-(Pyrrolidin-1-yl)ethoxy)benzaldehyde | HCID 976844 | 78.5% |
Reaction Steps
A mixture of 2.29 g of 4-(2-bromoethoxy)benzaldehyde, 1.42 g of pyrrolidine and 2.07 g of potassium carbonate in 8 ml of N,N-dimethylformamide was stirred at 60° C. for 2 hours. After cooling, water was added and the whole was extracted with ethyl acetate. The ethyl acetate layer was extracted with aqueous hydrochloric acid. The aqueous layer was made alkaline with potassium carbonate and extracted with ethyl acetate. The extract was washed with water, dried and evaporated. The residue was distilled to give 1.72 g of colorless oil, b.p. 170° C. (5 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983633 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-ecd9103d650245a79522e38e7d2fde7d |
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| Source note | uspto-grants-1991_01 |
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