HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453722Generated: October 30, 2026
Dimethylformamide → HCID 57855419, compound
https://huagongshe.com/reaction/453722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 53667594 | HCID 53667594 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 57855419 | HCID 57855419 | 60% |
Reaction Steps
A solution of a mixture E/Z of 2-(6,7-dihydrobenzo[b]thiophen-4(5H)-ylidene)acetic acid (0.38 g, 1.96 mmol) in thionyl chloride (3 mL) and a catalytic amount of DMF is refluxed for 5 min. The solvent is evaporated at reduced pressure and the residue is slowly added to a solution of N-methyl-N-benzylamine (0.24 g, 1.96 mmol) and triethylamine (0.5 mL) in dry CH2Cl2 (15 mL) cooled in an ice bath and stirred at room temperature monitoring the reaction by TLC. The solution is washed with water and the organic phase is dried and evaporated under reduced pressure, and the resulting crude is purified by column chromatography, giving (E)-N-benzyl-2-(6,7-dihydrobenzo[b]thien-4(5H)-ylidene)-N-methylacetamide (0.35 g, 1.17 mmol, 60%, viscous oil). 1H NMR (300 MHz, CDCl3): δ 1.95 (m, 2H), 2.87 (m, 4H), 3.00 (s, 3H), 4.65 (s, 2H), 6.34 (s, 1H), 7.04 (d, J=5.3 Hz, 1H), 7.09 (d, J=5.3 Hz, 1H), 7.23-7.38 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492563B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-4a99eb55efb0432397055411803723c1 |
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| Source note | uspto-grants-2013_07 |
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