HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500265Generated: October 30, 2026
Chloroform → 1-[2-Chloro-1-hydroxy-2-(1-quinolin-6-ylcyclopropyl)ethyl]pyrrolidine-2,5-dione
https://huagongshe.com/reaction/500265
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | D-Proline | HCID 8988 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | (1-Quinolin-6-ylcyclopropyl)acetaldehyde | HCID 86621505 | — |
| Product | 1-[2-Chloro-1-hydroxy-2-(1-quinolin-6-ylcyclopropyl)ethyl]pyrrolidine-2,5-dione | HCID 67223833 | — |
Reaction Steps
To a cooled (0° C.) mixture of (1-quinolin-6-ylcyclopropyl)acetaldehyde (9.9 g, 47 mmol), D-proline (1.1 g, 9.4 mmol) in chloroform (200 mL) was added N-chlorosuccinimide (6.26 g, 46.9 mmol). The mixture was stirred at 0° C. for 30 min and then gradually warmed to RT for 2 h. The reaction mixture was quenched with saturated sodium bicarbonate (25 mL) and extracted with EtOAc (3×100 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated. The precipitate formed was filtered to give the desired product. The filtrate was chromatographed on silica gel with EtOAc in methylene chloride (10%) to afford chloro(1-quinolin-6-ylcyclopropyl)acetaldehyde which was contaminated with pyrrolidine-2,5-dione (13.0 g), and automatically converted to the desired product after a few days. The total desired product obtained is 16 g. LCMS: (M+H)=345.0/347.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767675B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-9aa937dddc4e4064a602720070d4e865 |
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| Source note | uspto-grants-2010_08 |
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