HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 15670655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | HCID 12878387 | HCID 12878387 | — |
| Reactant | 3-(Benzyloxy)-4-bromophenol | HCID 15670654 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15670655 | HCID 15670655 | 72% |
Reaction Steps
A mixture of 21.8 g. (78 mmole) of 3-benzyloxy-4-bromophenol, 20.0 g. (82.6 mmole) of (S)-1-methyl-4-phenylbutyl methane sulfonate and 25.2 g. (200 mmole) of potassijm carbonate in 100 ml. dimethylformamide was heated at 85° C. for 13.5 hours. The reaction was cooled and added to 500 ml. water-500 ml. ether. The organic extract was washed with two 250 ml. portions of water, dried over magnesium sulfate and evaporated to an oil. The crude oil was purified via column chromatography on 750 g. of silica gel eluted with 10% ether-hexane to yield 23.9 g. (72%) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04371720 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-561a9a20f7264afeae31936999411acd |
| Source note | uspto-grants-1983_02 |