HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Oxetanemethanol, 3-(1,1-dimethylethyl)- → 3,5,8-Trioxabicyclo(2.2.2)octane, 1-tert-butyl-4-hex-5-ynyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Oxetanemethanol, 3-(1,1-dimethylethyl)- | HCID 180740 | — |
| Reactant | 6-Heptynoic acid | HCID 4377950 | — |
| Product | 3,5,8-Trioxabicyclo(2.2.2)octane, 1-tert-butyl-4-hex-5-ynyl- | HCID 180036 | — |
Reaction Steps
Using the procedure described in stage (vi) of Example I and starting from hept-6-ynoic acid and 3-t-butyl-3-hydroxymethyloxetane (2-t-butyl-2-hyddroxymethylpropan-1,3-diol was prepared by the method of Y. Ozoe and M. Eto Agric.Biol. Chem, 1982, 46, 411), 4-t-butyl-1-(hex-5-ynyl)-2,6,7-trioxabicyclo[2.2.2]octane was prepared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466710 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-20a8db03b743461ba24608e98ae96177 |
| Source note | uspto-grants-1995_11 |