Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | HCID 10216779 | HCID 10216779 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10308809 | HCID 10308809 | — |
Reaction Steps
The compound of example 21 (0.255 g, 0.581 mmol) was dissolved in methylene chloride (0.89 mL). To the solution of Example 21 was added trifluoromethane sulfonic acid (0.360 mL, 11.3 mmol) and anisole (0.190 mL, 1.74 mmol) at room temperature. After 45 minutes, the pH of the reaction mixture was adjusted to a pH of 9 to 10 with 1N NaOH, and then methylene chloride and water were added to the reaction flask. The contents of the flask were then transferred to a separatory funnel and extracted with methylene chloride (4×). The combined organic extracts were then dried with magnesium sulfate, filtered and concentrated. Further purification (10% ammonia in 2M solution of ethanol/ethyl acetate) yielded 0.157 g of the free amine product with some baseline impurities (80%). To purify further, the free amine was dissolved in diethyl ether/isopropanol, and then HCl in 2M solution of diethyl ether (1 eq) was added. After 30 minutes, the resulting precipitate was filtered to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129237B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-820a071b6a464143b4496beaf9854a3d |
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| Source note | uspto-grants-2006_10 |
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