HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,6-Dioxabicyclo[3.1.0]hexane → HCID 67808836, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,6-Dioxabicyclo[3.1.0]hexane | HCID 67511 | — |
| Reactant | HCID 14795713 | HCID 14795713 | — |
| Product | HCID 67808836 | HCID 67808836 | — |
Reaction Steps
3,5-Bis(1,1-dimethylethyl)benzenethiol (0.0078 mole) and the title compound of Example 18 (0.0074 mole) are added to a degassed (Argon) solution of 50% sodium hydroxide (5 ml) and isopropyl alcohol (50 ml). The reaction is heated to reflux for 24 hours. The reaction is cooled to room temperature and poured into water (125 ml). The solution is made acidic with 1N hydrochloric acid and extracted 3 times with 100 ml of diethyl ether. The combined diethyl ether extracts are dried over anhydrous magnesium sulfate, filtered and concentrated with a rotary evaporator. The product is purified by silica gel chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05476944 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-5c119260370043f1be68567f80e3736c |
| Source note | uspto-grants-1995_12 |