HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585818Generated: November 1, 2026
2-Thiophenecarboxaldehyde → 1-(3,4-Dimethoxyphenyl)ethan-1-amine
https://huagongshe.com/reaction/1585818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | (1s)-1-(3,4-dimethoxyphenyl)ethanamine | HCID 376091 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3,4-Dimethoxyphenyl)ethan-1-amine | HCID 3159243 | — |
Reaction Steps
To a solution of 43.8 g of (S)-1-(3,4-dimethoxyphenyl)ethylamine in 400 cm3 of dichloromethane are added, with stirring at a temperature in the region of 20° C., 16.8 cm3 of 2-thiophenecarboxaldehyde and 35 g of 4Å molecular sieves. The reaction mixture is stirred for 16 hours at a temperature in the region of 20° C., and then filtered through a sinter funnel containing Celite. The sinter funnel is washed with 3 times 50 cm3 of dichloromethane and the filtrates are combined and then concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. 45.95 g of (S)-N-(2-thienyl)-methylidene]-[1-(3,4-dimethoxyphenyl)ethylamine are thus obtained in the form of a colourless oil for which the characteristics are the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05939561 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-c03228919f6f4c2881d27cfbf7c44928 |
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| Source note | uspto-grants-1999_08 |
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