Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | HCID 178448075 | HCID 178448075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178448069 | HCID 178448069 | — |
Reaction Steps
To 0.6 g of sodium hydride (purity 60%) was added 30 ml of anhydrous N,N-dimethylformamide. While stirring sufficiently, to the solution was added a solution of 3.36 g of trans-4-(trans-4-propylcyclohexyl)cyclohexanol dissolved in 10 ml of anhydrous N,N-dimethylformamide. This mixture was continued to stirring at 50° C. for one hour and then 2.8 g of 4-methoxybenzyl chloride was added thereto, and the mixture was stirred and reacted at the same temperature for 3 hours with stirring. After completion of the reaction, 100 ml of water was added to the reaction mixture, the mixture was extracted with toluene, washed with a saturated NaCl aqua, dried and the solvent was removed under reduced pressure. The residue was purified by silica gel column to obtain 1.0 g of the targeted trans-4-(trans-4-propylcyclohexyl)cyclohexyl-4-methoxybenzyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05651919 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-ec4c507ea5d148a283236f81b0bac551 |
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| Source note | uspto-grants-1997_07 |
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