HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cycloheptanecarbonyl chloride → N-(Chroman-2-yl)methyl-cycloheptanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cycloheptanecarbonyl chloride | HCID 12556870 | — |
| Reactant | (3,4-dihydro-2H-1-benzopyran-2-yl)methanamine hydrochloride | HCID 22145477 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(Chroman-2-yl)methyl-cycloheptanecarboxamide | HCID 21843756 | — |
Reaction Steps
5.0 g (25 mmol) of 2-aminomethylchroman hydrochloride are dissolved in 50 ml of pyridine; 5.6 g (35 mmol) of cycloheptanecarbonyl chloride are added dropwise to this solution. After 1 hour at 50° C., the mixture is concentrated and the residue is partitioned between water and toluene/ethyl acetate 1:1. The organic phase is filtered over silica gel. The desired product is eluted with toluene/ethyl acetate 5:1. The amide obtained after concentration is further reacted directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962513 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-ef989f37aaed413fb2cdcc49a1ebf13e |
| Source note | uspto-grants-1999_10 |