Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Methoxybenzenethiol | HCID 12765 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 86614059 | HCID 86614059 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69057681 | HCID 69057681 | 103.7% |
Reaction Steps
To a solution of methyl 8-methyl-8-azabicyclo[3.2.1]oct-3-yl sulfate (Preparation 13, 35 g, 0.16 mol) in tetrahydrofuran (300 ml) was added with cooling to 0° C. sodium hydride (60% dispersion in oil, 7 g, 0.17 mol). After complete addition, 4-methoxybenzene thiol (23.8 g, 0.16 mol) was added in tetrahydrofuran (300 ml). The reaction mixture was heated under reflux for 2 h and then cooled to 30° C. and water (250 ml) was added. The tetrahydrofuran was removed in vacuo, dichloromethane was added and the layers separated. The organic layer washed with water, sodium hydroxide (1 M solution), water, and saturated brine before drying (Na2SO4). The organic extracts were concentrated in vacuo to give the title compound (43.7 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494992B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-21bef720a1cb43b3bd2ba80aa95c1958 |
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| Source note | uspto-grants-2009_02 |
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