Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Homoveratrylamine | HCID 8421 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23434938 | HCID 23434938 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11407338 | HCID 11407338 | 83.5% |
Reaction Steps
A solution of 10.8 g (0.04 mol) of the acyl chloride prepared in Example 5 in 20 ml of methylene chloride was added dropwise to a solution of 7.24 g (0.04 mol) of homoveratrylamine and 4.04 g 25 (0.04 mol) of triethylamine in 80 ml of methylene chloride. The solution was stirred for 3 hours at 20 to 25° C., and washed with 3 N sodium hydroxide solution and then with 10% by weight strength hydrochloric acid. The organic phase was freed from solvent, and 13.85 g of the title compound were obtained from the residue following chromatography on silica gel with cyclohehane [sic]/MtBE (3:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696607B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-2f8076c5fe6941bf9712c5357f0ade06 |
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| Source note | uspto-grants-2004_02 |
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