HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 54416378, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | HCID 15388862 | HCID 15388862 | — |
| Product | HCID 54416378 | HCID 54416378 | 73% |
Reaction Steps
Dissolved N-methyl-2-[6,11-dihydro-dibenzo[b,e]oxepin-11-yl]-pentanamine (0.50 g, 1.70 mmol)in 20 mL of dry THF. Added triethylamine (0.28 mL, 0.21 g, 2.02 mmol) and ethyl chloroformate (0.18 mL, 0.20 g, 1.86 mmol). Stirred at room temperature for 16 hours. Added water, and extracted with ether. Dried combined organic extracts with MgSO4, filtered, and evaporated. Purified crude product by flash chromatography on silica gel eluting with dichloromethane. Combined appropriate fractions, and evaporated to give 0.45 g (73% yield) of ethyl [2-(6,11 -dihydro-dibenzo[b,e]oxepin-1-yl)-pentyl]-methylcarbamate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574173 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-ff5a55f65fa642989a5dc5f96888099d |
| Source note | uspto-grants-1996_11 |