Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13882872 | HCID 13882872 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 14013750 | HCID 14013750 | 72.9% |
Reaction Steps
To 50 ml of dry THF at -78° C. was added 6.3 ml (0.045 mol) of diisopropylamine followed by 19 ml (0.043 mol) of 2.3M n-butyllithium in hexane. After stirring at -78° C. for 15 minutes, a solution of 13.0 g (0.036 mol) of product of Example 8 in 50 ml of dry THF was added. After stirring at -78° C. for one hour, small pieces of dry ice were added. The addition was stopped when the exotherm ceased. Stirring at -78° C. was continued for 1 hour and then the reaction mixture was allowed to warm up to room temperature in 11/2 hour. The reaction mixture was poured into 450 ml of H2O containing 50 ml of concentrated HCl, extracted with ether, dried (MgSO4) and concentrated in vacuo to a dark oil. This oil, 5.5 g (0.040 mol) of K2CO3 and 11.2 ml (0.180 mol) of methyl iodide in 125 ml of acetone was refluxed for 17 hours. The cooled reaction mixture was concentrated in vacuo. The residue was poured into water, extracted with ether, dried (MgSO4) and concentrated in vacuo to a dark oil which was kugelrohr distilled at 51 Pa, pot temperature 90° C., to give 11.01 g (72.9%) of product as a yellow oil, nD25 1.4484.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04835279 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-c4e254c1606742149836947b584845d1 |
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| Source note | uspto-grants-1989_05 |
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