HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 14597333, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Naphthalene, 2,7-bis(2-propynyloxy)- | HCID 12223656 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14597333 | HCID 14597333 | 45.3% |
Reaction Steps
Into a similar reaction vessel, as used in the abovementioned reaction, were placed 2.316 parts of t-BuOK and 13.108 parts of THF and to this, a mixture of 10,000 parts of 2,7-dipropargyloxynaphthalene and 23.333 parts of THF was added dropwise. The content was reacted at 50° C. for 60 minutes and then a deionized water was added to stop the reaction. THF layer and water layer were removed off by using an evaporator, and the residue was subjected to a column chromatography (silica gel 200 mesh) to obtain a purified 2,7-diallenyloxy naphthalene as white rystals (M.P. 80.5°-83.5° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05340931 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-38938d5ded6240c496cb83ebde3409da |
| Source note | uspto-grants-1994_08 |