Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 2-(Methylamino)ethanol | HCID 8016 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 23093472 | HCID 23093472 | 66.5% |
Reaction Steps
To a mixture of 2-(methylamino)ethanol (30.04 g) and ethyl acetate (90 mL) was added a mixture of di-tert-butyl dicarbonate (87.30 g) and ethyl acetate (10 mL) under ice-cooling. The reaction solution was stirred at room temperature for 1 hr, and benzoyl chloride (61.8 g) and pyridine (38.8 mL) were added thereeto under ice-cooling. The reaction solution was stirred at room temperature for 1 hr, and solid was filtered off. The solid was washed with ethyl acetate (100 mL), and the filtrate and washings were combined and washed with water (100 mL), then saturated saline (100 mL). The solution was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was dissolved in ethyl acetate (100 mL), and added 4N hydrogen chloride-ethyl acetate solution (200 mL), followed by stirring at room temperature for 30 minutes. Diethyl ether (100 mL) was added thereto, and solid was collected by filtration. After washing two times with ethyl acetate (100 mL), the solid was dried at 60° C. under reduced pressure to give title compound as white solid (57.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08449911B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-ee0f9e4719044a7a8b741cc8912468a6 |
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| Source note | uspto-grants-2013_05 |
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