HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895015Generated: October 25, 2026
2-Butyl-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester → HCID 66687362, compound
https://huagongshe.com/reaction/1895015
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Butyl-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester | HCID 86620858 | — |
| Reactant | HCID 178478192 | HCID 178478192 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66687362 | HCID 66687362 | 46% |
Reaction Steps
To a stirred solution of 2-butyl-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (0.753 g, 2.95 mmol) in THF (12 mL) at 0° C. and under nitrogen was added 3,4-dichlorophenylmagnesium bromide (11.8 mL of a 0.5 M solution in pentanes, 5.9 mmol) dropwise over 10 minutes. After 20 minutes, the reaction mixture was quenched by the addition of saturated aqueous NH4Cl (30 mL) then extracted with EtOAc. The combined extracts were washed with brine then dried (MgSO4), filtered and concentrated in vacuo to a yellow oil (1.9 g). Purification by chromatography (silica, 5-20% EtOAc in hexanes) gave 2-butyl-2-[(3,4-dichloro-phenyl)-hydroxy-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (0.548 g, 1.36 mmol, 46%) as a colourless gum and as an inseparable mixture of diastereomers
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513425B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-17f436ca55d24eb8ad85ecf788b0a371 |
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| Source note | uspto-grants-2013_08 |
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