HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29063Generated: October 27, 2026
Ethanol → (2S,3R)-1-((2E,4Z)-(S)-1,2-Dimethyl-hexa-2,4-dienyl)-3-(3-oxo-propyl) pyrrolidine-2-carboxylic acid ethyl ester
https://huagongshe.com/reaction/29063
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | (2S,3R)-3-But-3-enyl-1-((S)-1-phenyl-ethyl)-pyrrolidine-2-carboxylic acid ethyl ester | HCID 67003902 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | (2S,3R)-1-((2E,4Z)-(S)-1,2-Dimethyl-hexa-2,4-dienyl)-3-(3-oxo-propyl) pyrrolidine-2-carboxylic acid ethyl ester | HCID 86601083 | — |
Reaction Steps
(2S,3R)-3-But-3-enyl-1-((S)-1-phenyl-ethyl)-pyrrolidine-2-carboxylic acid ethyl ester(1.0 g, 3.32 mmol) is dissolved in EtOH(10 mL) with HCl(0.5 mL, 37%), and cooled to −70° C. Ozone gas is bubbled though the solution for about 10 min or until the solution is turned very light blue color. The nitrogen gas is bubbled though the solution for 15 min to remove excess ozone in the solution. To the cool solution is added Zn dust(0.43 g. 6.6 mmol) and HCl(0.5 mL, 37%), and stirred at r.t. for 20 min. After filtration the solution is diluted with 50 mL of CH2Cl2 and washed with saturated NaHCO3(10 mL) and 2×20 ml of water. After dried and concentrated, a colorless liquid(1.0 g) is obtained without further purification for next step reaction. (NMR and MS data confirmed, U-4117-51-30).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07419975B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-3f83b62510f14667887b4770ad407b35 |
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| Source note | uspto-grants-2008_09 |
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