HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468196Generated: November 1, 2026
Sodium Bromide → tert-butyl (3R)-3-formylpyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1468196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylate | HCID 1514340 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Catalyst | Tempo | HCID 2724126 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl (3R)-3-formylpyrrolidine-1-carboxylate | HCID 1514342 | 101% |
Reaction Steps
A solution of (R)-3-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester (50.0 g, 248.4 mmol, 1.0 eq.) in DCM (883 mL) was combined with TEMPO (1.9 g, 12.4 mmol, 0.05 eq.) and sodium bromide (2.6 g, 24.8 mmol, 0.1 eq.). The solution was cooled to 0° C. A solution of sodium hypochlorite (272.1 mL, 1.5 eq.) and sodium bicarbonate (31.2 g, 1.5 eq.) was added. Upon completion of the reaction, the mixture was extracted with DCM (3×200 mL) and dried over Na2SO4, to yield (R)-3-formylpyrrolidine-1-carboxylic acid t-butyl ester (50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000191B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-2a36b72d89a846a98cbfa45e42eb38c1 |
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| Source note | uspto-grants-2015_04 |
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