HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926Generated: October 23, 2026
Water → 2-(4-Cyanophenoxy)-1-methylethylamine
https://huagongshe.com/en/reaction/926
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Aminopropanol | HCID 5126 | — |
| Reactant | Benzonitrile, 4-bromo- | HCID 12162 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Cyanophenoxy)-1-methylethylamine | HCID 18972799 | 41% |
Reaction Steps
50.0 g of 2-amino-1-propanol was added dropwise to a stirred mixture of 29.3 g of 60% sodium hydride and 300 mL of dimethylformamide at 0° C. After the reaction mixture was stirred for 30 minutes at 0° C. a solution containing 121.2 g of 4-bromobenzonitrile dissolved in N,N-dimethylformamide was added dropwise to the reaction mixture. The resultant mixture was stirred for 20 hours at room temperature. After completion of the reaction, the resultant mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water and then dried over anhydrous magnesium sulfate. The ethyl acetate was removed under reduced pressure. The residue was distilled under reduced pressure to obtain 48.0 g of the desired product (yield 41%). Boiling point: 132° C./0.26 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723469 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-c11fa99e3841426fba61a399ec0730d1 |
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| Source note | uspto-grants-1998_03 |
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