HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 15227909, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-(1,2,3,4,10,14b-Hexahydrodibenzo[c,f]pyrazino[1,2-a]azepin-2-yl)ethoxyacetic acid | HCID 9928443 | — |
| Reactant | Chloroethyl carbonate | HCID 22631361 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15227909 | HCID 15227909 | 73.8% |
Reaction Steps
0.11 g of chloroethyl carbonate was added to a solution of 0.5 g of 2-(1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepin-2-yl)ethoxyacetic acid (prepared as described in Example 2) in 10 ml of chloroform containing 2% by volume ethanol, whilst ice-cooling, and the mixture was stirred at room temperature for 1 hour. At the end of this time, it was washed with water, and the solvent was removed by distillation under reduced pressure. The resulting residue was subjected to column chromatography through silica gel eluted with ethyl acetate, to give 0.25 g of the title compound as a colorless oil. The infrared absorption spectrum of this compound is identical with that of the compound prepared as described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05476848 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-ef308a88bcf74427884a4df2c177b299 |
| Source note | uspto-grants-1995_12 |