Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Benzene, 1-(chloromethyl)-2-fluoro- | HCID 9580 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13215602 | HCID 13215602 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 53795816 | HCID 53795816 | 88.9% |
Reaction Steps
396.0 g. (4.5 mol) of cis-1,2-cyclobutanediol and 650.3 g (4.5 mol) of 2-fluorobenzyl chloride were dissolved in 2.5 liters of dimethylsulphoxide, and 270 g (6.75 mol) of sodium hydroxide powder were added in portions at room temperature, whilst cooling with ice. The mixture was stirred at room temperature for 6 hours and 958.5 g (6.75 mol) of methyl iodide and, in portions, 270 g (6.75 mol) of sodium hydroxide powder were then added, whilst cooling. Thereafter, the reaction mixture was again stirred at room temperature for 6 hours and discharged onto 10 liters of ice-water. The mixture was extracted three times with 5 liters of petroleum ether each time and the combined organic phases were dried over sodium sulphate and concentrated by distilling off the solvent. 840 g (88.9% of theory) of cis-1-(2-fluorobenzyloxy)-2-methoxy-cyclobutane of refractive index nD21 =1.4948 were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04282388 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-6511cefe66a34f67b9747b46a63c9f90 |
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| Source note | uspto-grants-1981_08 |
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