HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644819Generated: October 31, 2026
Triacetoxyperiodinane → 2-(4-Fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1644819
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | 2-(4-Fluoro-phenyl)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 66773577 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 86635623 | 106.6% |
Reaction Steps
To 2-(4-fluoro-phenyl)-2-hydroxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (3.9 g) in a round bottom flask was added Dess-Martin periodinane solution (47 mL of a 15% solution in DCM, CAS [87413-09-0]) and the reaction mixture was stirred for 5 hours at RT. The reaction mixture was then quenched with saturated aqueous sodium thiosulfate solution (25 mL) and stirred a further 20 minutes. The phases were separated and the aqueous was extracted with further DCM (25 mL). The combined organic phases were washed with saturated sodium bicarbonate solution and dried over sodium sulfate. Filtration of the drying agent and evaporation of the volatiles in vacuo afforded the desired 2-(4-fluoro-phenyl)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (4.13 g, MS (ES+): 294.1 (MH+)) as a brown solid which was taken into the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124636B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-0743f584853140efbd7affb7db0cec47 |
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| Source note | uspto-grants-2012_02 |
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