HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide → 5,7,8,9-tetrahydro-6H-[1,3]dioxolo[4,5-h][3]benzazepin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide | HCID 84998 | — |
| Reactant | 6-(2-Aminoethyl)-4,5-methylenedioxy phenyl-acetic acid hydrochloride | HCID 68122847 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,7,8,9-tetrahydro-6H-[1,3]dioxolo[4,5-h][3]benzazepin-6-one | HCID 13092509 | — |
Reaction Steps
Similarly, 0.005 moles (1.3 grams) of 6-(2-aminoethyl)-4,5-methylenedioxy phenyl-acetic acid hydrochloride were dissolved in 15 ml of water and to this solution was added 2.12 grams of 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide methotoluenesulfonate in 20 ml of water. After 2 hours at room temperature the precipitate that had formed was filtered off, washed and dried to yield 1,3,4,5-tetrahydro-7,8-methylenedioxy-2H-3-benzazepin-2-one, m.p. 236°-237°. After recrystallization from ether the product melted at 238°-239°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065473 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-cedf853a25d14afc95274d438ae71bbb |
| Source note | uspto-grants-1977_12 |