HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253515Generated: November 2, 2026
Pyridine → (+-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehyde
https://huagongshe.com/reaction/1253515
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | tert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate | HCID 5237175 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehyde | HCID 4692112 | — |
Reaction Steps
To a solution of pyridine (9.5 g, 0.12 mol) in dichloromethane (150 mL) was added chromium trioxide (6.0 g, 0.06 mol). The internal reaction temperature was not allowed to exceed 20° C. during the addition. After 15 minutes, the stirred mixture was charged with a solution of tert-butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate (2.0 g, 10 mmol) in dichloromethane (30 mL). After 15 minutes, the solution was decanted from the reaction vessel which was washed with dichloromethane (200 mL). The organics were combined, washed with 5% aqueous sodium hydroxide (3×100 mL), then washed with 5% hydrochloric acid (100 mL), then washed with 5% aqueous sodium bicarbonate (100 mL), and finally washed with 5% aqueous sodium chloride (100 mL). The organics were dried over magnesium sulfate, filtered, and concentrated in vacuo to afford tert-butyl 3-formylpyrrolidine-1-carboxylate that was used without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455477B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-c9eb831ad1504dbf8ff82468b344d09c |
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| Source note | uspto-grants-2013_06 |
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