HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexyl bromide → HCID 20380992, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexyl bromide | HCID 7960 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 20380987 | HCID 20380987 | — |
| Product | HCID 20380992 | HCID 20380992 | — |
Reaction Steps
5.0 g (0.0262 mole) of 4-benzoyl oxazolidin-2-one dissolved in 100 ml of absolute tetrahydrofuran are added dropwise while cooling with ice to a Grignard solution prepared from 12.8 ml (0.127 mole) of bromocyclohexane and 2.98 g (0.128 gram equivalent) of magnesium in 150 ml of absolute tetrahydrofuran. This solution is stirred for 2 hours at 60° C., subsequently hydrolysed with approximately 500 ml of a saturated ammonium chloride solution and repeatedly extracted with chloroform. The organic phases are combined, dried over Na2SO4 and concentrated in a rotary evaporator. The oil is taken up in ether. The crystals formed are filtered off under suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04179442 |
| Source dataset | uspto-grants-1979_12 |
| ORD ID | ord-2b58e46b684b449fa2dabacd566ede4a |
| Source note | uspto-grants-1979_12 |