HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 19705272, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(Trifluoromethyl)benzaldehyde | HCID 67990 | — |
| Reactant | 8-bromo-1,4-dioxaspiro[4.5]decane | HCID 13765129 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19705272 | HCID 19705272 | — |
Reaction Steps
This compound is prepared in a manner analogous to that of Step B of Example 6, using 22.1 grams (0.09 mole) of the Grignard reagent of 8-bromo-1,4-dioxaspiro[4.5]decane and 17.4 grams (0.10 mole) of 3-trifluoromethylbenzaldehyde in tetrahydrofuran. Upon completion of the reaction, the reaction mixture is poured into a mixture of 100 grams of ice, 100 mL of an aqueous solution saturated with ammonium chloride, and 200 mL of diethyl ether. This mixture is filtered and the organic layer is separated. The organic layer is concentrated under reduced pressure, yielding [(1,4-dioxaspiro[4.5]decan-8-yl)(3-trifluoromethylphenyl)]methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05712281 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-1355eb88ccb34aedbf99e406539765fd |
| Source note | uspto-grants-1998_01 |