Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | HCID 86661757 | HCID 86661757 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66726783 | HCID 66726783 | — |
Reaction Steps
5.4 mL of allylamine was added to a tetrahydrofuran (100 mL) solution of 8.2 g of (R)-2-(2-nitrophenylsulfonamido)propyl methanesulfonate, and the mixture was stirred at 80° C. for 16 hours. After the completion of reaction, the reaction solution was returned to room temperature, and 100 mL of saturated saline was added thereto. From this mixed solution, two extractions were performed with 100 mL of ethyl acetate. The extract was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated, and the obtained crude product was purified by silica gel column chromatography (ethyl acetate:hexane=1:1) to obtain 7 g of the compound of interest as a yellow oil (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08951997B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-d297c204e8924e7ba80a1970f88affdd |
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| Source note | uspto-grants-2015_02 |
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