HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420846Generated: October 30, 2026
Hydrochloric Acid → HCID 62069033, compound
https://huagongshe.com/reaction/420846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methoxy-1-phenylethanone | HCID 77698 | — |
| Reactant | tert-butyl N-(pyrrolidin-3-yl)carbamate | HCID 2757234 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 62069033 | HCID 62069033 | — |
Reaction Steps
3-t-Butoxycarbonylaminopyrrolidine (560 mg) was dissolved in methanol (5 ml), the solution was added with acetic acid (170 μl), 2-methoxyacetophenone (140 μl) and sodium cyanoborohydride (45 mg), and the mixture was stirred at 50° C. for 20 hours. The reaction mixture was added with 5 N hydrochloric acid (10 ml), the mixture was stirred at room temperature for 2 hours, and then made basic with potassium carbonate, and methanol was evaporated under reduced pressure. The reaction mixture was added with chloroform, the layers were separated, the organic layer was dried over anhydrous magnesium sulfate and filtered, and then the filtrate was concentrated under reduced pressure to obtain the title compound (83 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097708B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c564d8dc9e3349928916924c13524ae6 |
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| Source note | uspto-grants-2012_01 |
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