HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386520Generated: November 1, 2026
N-Methylbenzylamine → HCID 21181564, compound
https://huagongshe.com/reaction/1386520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 21181672 | HCID 21181672 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21181564 | HCID 21181564 | 76.6% |
Reaction Steps
To a mixture of the product compound of Example 8, Step (b) (508 mg, 2.00 mmoles), methyl benzylamine (484 mg, 4.00 mmoles), and tetra-n-butylamrnonium iodide (74 mg) in dry dimethylformamide (2.0 mL) was added anhydrous potassium carbonate (552 mg, 4.00 imol). The mixture was stirred overnight at 80-85°. After cooling, the mixture was partitioned between diethyl ether and water, the aqueous layer was extracted with ether, the combined organic extracts were washed with brine, dried over sodium sulfate, filtered and the solvent evaporated. Chromatography of the residue over silica gel using 25% ethyl acetate-hexane as eluent gave a compound (540 mg) as an oil which was characterized by NMR, as follows: 1H NMR(CD2Cl2) d 7.63-6.95(m, 9H), 1.22(d, 3H), 0.82(d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265439B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-6f338d27eb294897bb6b07a5eabd742c |
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| Source note | uspto-grants-2001_07 |
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