HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → (4S)-1,1-diethoxy-4-(2-tetrahydropyranyloxy)-2-nonyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | (3S)-3-(2-tetrahydropyranyloxy)-1-octyne | HCID 11805967 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4S)-1,1-diethoxy-4-(2-tetrahydropyranyloxy)-2-nonyne | HCID 68121838 | — |
Reaction Steps
A solution of ethylmagnesium bromide in 400 ml. of ether is prepared in the usual manner from magnesium (12.2 g., 0.5 mole) and ethyl bromide (56.5 g., 0.52 mole). To this solution, (3S)-3-(2-tetrahydropyranyloxy)-1-octyne (88.2 g., 0.42 mole) is added dropwise with stirring during one hour. The reaction mixture is stirred an additional 45 minutes, and there is added triethyl orthoformate (81.4 g., 0.55 mole) dropwise during 30 minutes. The mixture is then refluxed 16 hours. It is poured into 500 ml. of iced saturated ammonium chloride solution. The oily product is taken up in ether, washed with water, dried over sodium sulfate and distilled to obtain (4S)-1,1-diethoxy-4-(2-tetrahydropyranyloxy)-2-nonyne.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055597 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-85331ebb9f9c4600a55e39208e4c482a |
| Source note | uspto-grants-1977_10 |